Climara ESTRADIOL

CLIMARA (ESTRADIOL) 0.025 mg

BAYER HEALTHCARE PHARMACEUTICALS INC. FDA Rx Only

Climara (estradiol transdermal system), is designed to release estradiol continuously upon application to intact skin. Six (6.5, 9.375, 12.5, 15, 18.75 and 25 cm 2 ) systems are available to provide nominal in vivo delivery of 0.025, 0.0375, 0.05, 0.06, 0.075 or 0.1 mg respectively of estradiol per day. The period of use is 7 days. Each system has a contact surface area of either 6.5, 9.375, 12.5, 15, 18.75 or 25 cm 2 , and contains 2, 2.85, 3.8, 4.55, 5.7 or 7.6 mg of estradiol USP respectively. The composition of the systems per unit area is identical. Estradiol USP is a white, crystalline powder, chemically described as estra-1,3,5(10)-triene-3, 17β-diol. It has an empirical formula of C 18 H 24 O 2 and molecular weight of 272.38. The structural formula is: The Climara transdermal system comprises three layers. Proceeding from the visible surface toward the surface attached to the skin, these layers are: 1. A translucent polyethylene film. 2. An acrylate adhesive matrix containing estradiol USP. 3. A protective liner of siliconized or fluoropolymer-coated polyester film is attached to the adhesive surface and must be removed before the system can be used. The active component of the transdermal system is estradiol. The remaining components of the transdermal system (acrylate copolymer adhesive, fatty acid esters, and polyethylene backing) are pharmacologically inactive. Chemical Structure Patch Diagram

DIVIGEL ESTRADIOL

DIVIGEL (ESTRADIOL) 1.25 g Gel

VERTICAL PHARMACEUTICALS, LLC FDA Rx Only

Divigel (estradiol gel) 0.1 percent, is a clear, colorless gel, which is odorless when dry. It is designed to deliver sustained circulating concentrations of estradiol when applied once daily to the skin. The gel is applied to a small area (200 cm 2 ) of the thigh in a thin layer. Divigel is available in five doses of 0.25, 0.5, 0.75, 1.0, and 1.25 grams for topical application (corresponding to 0.25, 0.5, 0.75, 1.0, and 1.25 mg estradiol, respectively). The active component of the topical gel is estradiol. Estradiol is a white crystalline powder, chemically described as estra-1,3,5(10)-triene-3,17ß-diol. It has an empirical formula of C 18 H 24 O 2 and molecular weight of 272.39. The structural formula is: Divigel Chemical Structure The remaining components of the gel (carbomer, ethanol, propylene glycol, purified water, and triethanolamine) are pharmacologically inactive. Divigel Chemical Structure

DOTTI ESTRADIOL

DOTTI (ESTRADIOL) 0.025 mg

AMNEAL PHARMACEUTICALS LLC FDA Rx Only

DOTTI (estradiol transdermal system, USP) contains estradiol, USP in a multipolymeric adhesive. The system is designed to release estradiol, USP continuously upon application to intact skin. Five dosage strengths of DOTTI are available to provide nominal in vivo delivery rates of 0.025, 0.0375, 0.05, 0.075, or 0.1 mg of estradiol, USP per day via the skin. Each corresponding system has an active surface area of 1.89, 2.83, 3.78, 5.66, or 7.55 cm 2 and contains 0.314, 0.470, 0.627, 0.940, or 1.253 mg of estradiol USP, respectively. The composition of the systems per unit area is identical. Estradiol, USP is a white to practically white powder, chemically described as estra-1,3,5 (10)- triene-3,17β-diol. The structural formula is: The molecular formula of estradiol, USP is C 18 H 24 0 2 . The molecular weight is 272.39 g/mol. DOTTI is comprised of 3 layers. Proceeding from the visible surface toward the surface attached to the skin, these layers are (1) polyester and ethylene vinyl acetate copolymer film (2) an adhesive formulation containing estradiol USP, acrylic adhesive, silicone adhesive, oleyl alcohol, NF, povidone, USP and dipropylene glycol, and (3) a polyester release liner which is attached to the adhesive surface and must be removed before the system can be used. The active component of the system is estradiol, USP. The remaining components of the system are pharmacologically inactive. FDA approved acceptance criteria for dissolution test specifications differ from USP. 1 2

DOTTI ESTRADIOL

DOTTI (ESTRADIOL) 0.025 mg

BRYANT RANCH PREPACK FDA Rx Only

DOTTI (estradiol transdermal system, USP) contains estradiol, USP in a multipolymeric adhesive. The system is designed to release estradiol, USP continuously upon application to intact skin. Five dosage strengths of DOTTI are available to provide nominal in vivo delivery rates of 0.025, 0.0375, 0.05, 0.075, or 0.1 mg of estradiol, USP per day via the skin. Each corresponding system has an active surface area of 1.89, 2.83, 3.78, 5.66, or 7.55 cm 2 and contains 0.314, 0.470, 0.627, 0.940, or 1.253 mg of estradiol USP, respectively. The composition of the systems per unit area is identical. Estradiol, USP is a white to practically white powder, chemically described as estra-1,3,5 (10)- triene-3,17β-diol. The structural formula is: The molecular formula of estradiol, USP is C 18 H 24 0 2 . The molecular weight is 272.39 g/mol. DOTTI is comprised of 3 layers. Proceeding from the visible surface toward the surface attached to the skin, these layers are (1) polyester and ethylene vinyl acetate copolymer film (2) an adhesive formulation containing estradiol USP, acrylic adhesive, silicone adhesive, oleyl alcohol, NF, povidone, USP and dipropylene glycol, and (3) a polyester release liner which is attached to the adhesive surface and must be removed before the system can be used. The active component of the system is estradiol, USP. The remaining components of the system are pharmacologically inactive. FDA approved acceptance criteria for dissolution test specifications differ from USP.

DOTTI ESTRADIOL

DOTTI (ESTRADIOL) 0.025 mg

BRYANT RANCH PREPACK FDA Rx Only

DOTTI (estradiol transdermal system, USP) contains estradiol, USP in a multipolymeric adhesive. The system is designed to release estradiol, USP continuously upon application to intact skin. Five dosage strengths of DOTTI are available to provide nominal in vivo delivery rates of 0.025, 0.0375, 0.05, 0.075, or 0.1 mg of estradiol, USP per day via the skin. Each corresponding system has an active surface area of 1.89, 2.83, 3.78, 5.66, or 7.55 cm 2 and contains 0.314, 0.470, 0.627, 0.940, or 1.253 mg of estradiol USP, respectively. The composition of the systems per unit area is identical. Estradiol, USP is a white to practically white powder, chemically described as estra-1,3,5 (10)- triene-3,17β-diol. The structural formula is: The molecular formula of estradiol, USP is C 18 H 24 0 2 . The molecular weight is 272.39 g/mol. DOTTI is comprised of 3 layers. Proceeding from the visible surface toward the surface attached to the skin, these layers are (1) polyester and ethylene vinyl acetate copolymer film (2) an adhesive formulation containing estradiol USP, acrylic adhesive, silicone adhesive, oleyl alcohol, NF, povidone, USP and dipropylene glycol, and (3) a polyester release liner which is attached to the adhesive surface and must be removed before the system can be used. The active component of the system is estradiol, USP. The remaining components of the system are pharmacologically inactive. FDA approved acceptance criteria for dissolution test specifications differ from USP.

DOTTI ESTRADIOL

DOTTI (ESTRADIOL) 0.025 mg

BRYANT RANCH PREPACK FDA Rx Only

DOTTI (estradiol transdermal system, USP) contains estradiol, USP in a multipolymeric adhesive. The system is designed to release estradiol, USP continuously upon application to intact skin. Five dosage strengths of DOTTI are available to provide nominal in vivo delivery rates of 0.025, 0.0375, 0.05, 0.075, or 0.1 mg of estradiol, USP per day via the skin. Each corresponding system has an active surface area of 1.89, 2.83, 3.78, 5.66, or 7.55 cm 2 and contains 0.314, 0.470, 0.627, 0.940, or 1.253 mg of estradiol USP, respectively. The composition of the systems per unit area is identical. Estradiol, USP is a white to practically white powder, chemically described as estra-1,3,5 (10)- triene-3,17β-diol. The structural formula is: The molecular formula of estradiol, USP is C 18 H 24 0 2 . The molecular weight is 272.39 g/mol. DOTTI is comprised of 3 layers. Proceeding from the visible surface toward the surface attached to the skin, these layers are (1) polyester and ethylene vinyl acetate copolymer film (2) an adhesive formulation containing estradiol USP, acrylic adhesive, silicone adhesive, oleyl alcohol, NF, povidone, USP and dipropylene glycol, and (3) a polyester release liner which is attached to the adhesive surface and must be removed before the system can be used. The active component of the system is estradiol, USP. The remaining components of the system are pharmacologically inactive. FDA approved acceptance criteria for dissolution test specifications differ from USP.

DOTTI ESTRADIOL

DOTTI (ESTRADIOL) 0.025 mg

BRYANT RANCH PREPACK FDA Rx Only

DOTTI (estradiol transdermal system, USP) contains estradiol, USP in a multipolymeric adhesive. The system is designed to release estradiol, USP continuously upon application to intact skin. Five dosage strengths of DOTTI are available to provide nominal in vivo delivery rates of 0.025, 0.0375, 0.05, 0.075, or 0.1 mg of estradiol, USP per day via the skin. Each corresponding system has an active surface area of 1.89, 2.83, 3.78, 5.66, or 7.55 cm 2 and contains 0.314, 0.470, 0.627, 0.940, or 1.253 mg of estradiol USP, respectively. The composition of the systems per unit area is identical. Estradiol, USP is a white to practically white powder, chemically described as estra-1,3,5 (10)- triene-3,17β-diol. The structural formula is: The molecular formula of estradiol, USP is C 18 H 24 0 2 . The molecular weight is 272.39 g/mol. DOTTI is comprised of 3 layers. Proceeding from the visible surface toward the surface attached to the skin, these layers are (1) polyester and ethylene vinyl acetate copolymer film (2) an adhesive formulation containing estradiol USP, acrylic adhesive, silicone adhesive, oleyl alcohol, NF, povidone, USP and dipropylene glycol, and (3) a polyester release liner which is attached to the adhesive surface and must be removed before the system can be used. The active component of the system is estradiol, USP. The remaining components of the system are pharmacologically inactive. FDA approved acceptance criteria for dissolution test specifications differ from USP.

DOTTI ESTRADIOL

DOTTI (ESTRADIOL) 0.025 mg

BRYANT RANCH PREPACK FDA Rx Only

DOTTI (estradiol transdermal system, USP) contains estradiol, USP in a multipolymeric adhesive. The system is designed to release estradiol, USP continuously upon application to intact skin. Five dosage strengths of DOTTI are available to provide nominal in vivo delivery rates of 0.025, 0.0375, 0.05, 0.075, or 0.1 mg of estradiol, USP per day via the skin. Each corresponding system has an active surface area of 1.89, 2.83, 3.78, 5.66, or 7.55 cm 2 and contains 0.314, 0.470, 0.627, 0.940, or 1.253 mg of estradiol USP, respectively. The composition of the systems per unit area is identical. Estradiol, USP is a white to practically white powder, chemically described as estra-1,3,5 (10)- triene-3,17β-diol. The structural formula is: The molecular formula of estradiol, USP is C 18 H 24 0 2 . The molecular weight is 272.39 g/mol. DOTTI is comprised of 3 layers. Proceeding from the visible surface toward the surface attached to the skin, these layers are (1) polyester and ethylene vinyl acetate copolymer film (2) an adhesive formulation containing estradiol USP, acrylic adhesive, silicone adhesive, oleyl alcohol, NF, povidone, USP and dipropylene glycol, and (3) a polyester release liner which is attached to the adhesive surface and must be removed before the system can be used. The active component of the system is estradiol, USP. The remaining components of the system are pharmacologically inactive. FDA approved acceptance criteria for dissolution test specifications differ from USP.

ELESTRIN ESTRADIOL

ELESTRIN (ESTRADIOL) 0.52 mg Gel

VIATRIS SPECIALTY LLC FDA Rx Only

ELESTRIN (estradiol gel) contains 0.06% of estradiol, in a colorless, non-staining hydroalcoholic gel base. One pump actuation delivers ELESTRIN in a unit dose of 0.52 mg of estradiol in 0.87 g of gel. Estradiol is a white crystalline powder, chemically described as estra-1,3,5(10)-triene-3,17-diol, (17β)-. It has a molecular formula of C 18 H 24 O 2 •½H 2 O and molecular weight of 281.4. The structural formula is: The active component of ELESTRIN is estradiol. The remaining components of the gel (ethanol, propylene glycol, diethylene glycol monoethyl ether, carbomer homopolymer type C, triethanolamine, edetate disodium, and purified water) are pharmacologically inactive. Elestrin Structural Formula

ESTRACE ESTRADIOL

ESTRACE (ESTRADIOL) 42.5 g

A-S MEDICATION SOLUTIONS FDA Rx Only

Each gram of ESTRACE (estradiol vaginal cream USP 0.01%) contains 0.1 mg estradiol in a nonliquefying base containing purified water, propylene glycol, stearyl alcohol, white ceresin wax, mono- and di-glycerides, hypromellose 2208 (4000 cps), sodium lauryl sulfate, methylparaben, edetate di-sodium and tertiary -butylhydroquinone. Estradiol is chemically described as estra-1,3,5(10)-triene-3, 17(beta)-diol. It has an empirical formula of C 18 H 24 O 2 and molecular weight of 272.37. The structural formula is: The structural formula for ESTRACE (estradiol vaginal cream, USP, 0.01%) contains 0.1 mg estradiol in a nonliquefying base containing purified water, propylene glycol, stearyl alcohol, white ceresin wax, mono- and di-glycerides, hypromellose 2208 (4000 cps), sodium lauryl sulfate, methylparaben, edetate di-sodium and tertiary-butylhydroquinone. Estradiol is chemically described as estra-1,3,5(10)-triene-3, 17(beta)-diol. It has an empirical formula of C18H24O2 and molecular weight of 272.37.

ESTRACE ESTRADIOL

ESTRACE (ESTRADIOL) 42.5 g

ALLERGAN, INC. FDA Rx Only

Each gram of ESTRACE (estradiol vaginal cream USP 0.01%) contains 0.1 mg estradiol in a nonliquefying base containing purified water, propylene glycol, stearyl alcohol, white ceresin wax, mono- and di-glycerides, hypromellose 2208 (4000 cps), sodium lauryl sulfate, methylparaben, edetate di-sodium and tertiary -butylhydroquinone. Estradiol is chemically described as estra-1,3,5(10)-triene-3, 17(beta)-diol. It has an empirical formula of C 18 H 24 O 2 and molecular weight of 272.37. The structural formula is: The structural formula for ESTRACE (estradiol vaginal cream, USP, 0.01%) contains 0.1 mg estradiol in a nonliquefying base containing purified water, propylene glycol, stearyl alcohol, white ceresin wax, mono- and di-glycerides, hypromellose 2208 (4000 cps), sodium lauryl sulfate, methylparaben, edetate di-sodium and tertiary-butylhydroquinone. Estradiol is chemically described as estra-1,3,5(10)-triene-3, 17(beta)-diol. It has an empirical formula of C18H24O2 and molecular weight of 272.37.

Estradiol ESTRADIOL

ESTRADIOL 0.5 mg

PREFERRED PHARMACEUTICALS INC. FDA Rx Only

Estradiol Tablets, USP for oral administration contains 0.5, 1 or 2 mg of micronized estradiol, USP per tablet. Estradiol, USP (17β-estradiol) is a white, crystalline solid, chemically described as estra-1,3,5,(10)-triene-3, 17β-diol. The structural formula is: C 18 H 24 O 2 M.W. 272.38 Inactive Ingredients: Colloidal silicon dioxide, corn starch, dibasic calcium phosphate, lactose monohydrate, magnesium stearate, and sodium starch glycolate. In addition, the 1 mg also contains FD&C blue no. 1 aluminum lake and D&C red no. 27 aluminum lake. The 2 mg also contains FD&C blue no. 1 aluminum lake and FD&C yellow no. 5 (tartrazine) aluminum lake. structual formula

Estradiol ESTRADIOL

ESTRADIOL 0.5 mg

ANI PHARMACEUTICALS, INC. FDA Rx Only

Estradiol Tablets USP for oral administration contains 0.5, 1 or 2 mg of micronized estradiol, USP per tablet. Estradiol, USP (17β-estradiol) is a white to practically white powder, chemically described as estra-1,3,5,(10)-triene-3, 17β-diol. The structural formula is: C 18 H 24 O 2 M.W. 272.38 Inactive Ingredients: Colloidal silicon dioxide, corn starch, microcrystalline cellulose, lactose monohydrate, magnesium stearate, and sodium starch glycolate. In addition, the 1 mg also contains FD&C blue no. 1 aluminum lake and D&C red no. 27 aluminum lake. The 2 mg also contains FD&C blue no. 1 aluminum lake and D&C yellow no. 10 aluminum lake. FDA approved dissolution test specifications differ from USP. structure

estradiol ESTRADIOL

ESTRADIOL 0.025 mg

ZYDUS PHARMACEUTICALS USA INC. FDA Rx Only

Estradiol Transdermal System, USP is designed to release estradiol continuously upon application to intact skin. Six (7.5, 11.25, 15, 18, 22.5 and 30 cm 2 ) systems are available to provide nominal in vivo delivery of 0.025, 0.0375, 0.05, 0.06, 0.075 or 0.1 mg respectively of estradiol per day. The period of use is 7 days. Each system has a contact surface area of either 7.5, 11.25, 15, 18, 22.5 or 30 cm 2 , and contains 1.888, 2.832, 3.777, 4.532, 5.665 or 7.553 mg of estradiol USP respectively. The composition of the systems per unit area is identical. Estradiol USP is a white or creamy white, small crystals or crystalline powder, odorless, stable in air and hygroscopic. Estradiol USP is chemically described as estra-1,3,5(10)-triene-3, 17ß-diol. It has an empirical formula of C 18 H 24 O 2 and molecular weight of 272.38. The structural formula is: The Estradiol Transdermal System, USP comprises three layers. Proceeding from the visible surface toward the surface attached to the skin, these layers are: A translucent polyethylene film. An acrylate adhesive matrix containing estradiol USP. A protective liner of silicone coated polyester film is attached to the adhesive surface and must be removed before the system can be used. Cross Section of the System Estradiol Transdermal System, USP is packaged with additional pieces of protective film above and below the system within each pouch. These are discarded at the time of use. The active component of the system is estradiol USP. The remaining components of the system (acrylic adhesive, colloidal silicon dioxide, ethyl oleate, glyceryl monolaurate, isopropyl myristate, povidone and polyethylene backing) are pharmacologically inactive. FDA approved drug release test specifications differ from USP. Estradiol Transdermal System Estradiol Transdermal System

estradiol ESTRADIOL

ESTRADIOL 0.014 mg

ZYDUS PHARMACEUTICALS USA INC. FDA Rx Only

Estradiol transdermal system, USP is designed to provide nominal in vivo delivery of 0.014 mg of estradiol per day continuously upon application to intact skin. The period of use is 7 days. The transdermal system has a contact surface area of 3.9 cm 2 , and contains 0.982 mg of estradiol USP. Estradiol USP is a white, crystalline powder, chemically described as estra-1,3,5(10)-triene-3, 17ß-diol. It has an empirical formula of C 18 H 24 O 2 and molecular weight of 272.38. The structural formula is: The estradiol transdermal system, USP comprises three layers. Proceeding from the visible surface toward the surface attached to the skin, these layers are: 1. a translucent polyethylene film. 2. an acrylate adhesive matrix containing estradiol USP. 3. A protective liner of silicon coated polyester film is attached to the adhesive surface and must be removed before the transdermal system can be used. Cross Section of the System: Estradiol transdermal system, USP is packaged with additional pieces of protective film above and below the system within each pouch. These are discarded at the time of use. The active component of the transdermal system is estradiol USP. The remaining components of the transdermal system (acrylic adhesive, colloidal silicon dioxide, ethyl oleate, glyceryl monolaurate, isopropyl myristate, povidone, and polyethylene backing) are pharmacologically inactive. FDA approved drug release test specifications differ from USP. Estradiol Transdermal System, 14 mcg/day Estradiol Transdermal System, 14 mcg/ day

estradiol ESTRADIOL

ESTRADIOL

ZYDUS LIFESCIENCES LIMITED FDA Rx Only

Summary not available yet.

ESTRADIOL ESTRADIOL

ESTRADIOL 1.25 g Gel

BRYANT RANCH PREPACK FDA Rx Only

Estradiol gel 0.1 percent, is a clear, colorless gel, which is odorless when dry. It is designed to deliver sustained circulating concentrations of estradiol when applied once daily to the skin. The gel is applied to a small area (200 cm 2 ) of the thigh in a thin layer. Estradiol gel is available in five doses of 0.25, 0.5, 0.75, 1.0, and 1.25 grams for topical application (corresponding to 0.25, 0.5, 0.75, 1.0, and 1.25 mg estradiol, respectively). The active component of the topical gel is estradiol. Estradiol is a white crystalline powder, chemically described as estra-1,3,5(10)-triene-3,17β-diol. It has an empirical formula of C 18 H 24 O 2 and molecular weight of 272.39. The structural formula is: The remaining components of the gel (carbomer, ethanol (62.03% v/v), propylene glycol, purified water, and triethanolamine) are pharmacologically inactive.

ESTRADIOL ESTRADIOL

ESTRADIOL 1 mg

PREFERRED PHARMACEUTICALS INC. FDA Rx Only

Estradiol tablets, USP for oral administration contains 0.5, 1 or 2 mg of micronized estradiol, USP per tablet. Estradiol, USP (17β-estradiol) is a white, crystalline solid, chemically described as estra-1,3,5,(10)-triene-3, 17β-diol. The structural formula is: In addition, each tablet for oral administration contains the following inactive ingredients: lactose monohydrate, magnesium stearate, microcrystalline cellulose and sodium starch glycolate. Structure formula.jpg

Estradiol ESTRADIOL

ESTRADIOL

A-S MEDICATION SOLUTIONS FDA Rx Only

Estradiol Tablets USP for oral administration contains 0.5, 1 or 2 mg of micronized estradiol, USP per tablet. Estradiol, USP (17β-estradiol) is a white to practically white powder, chemically described as estra-1,3,5,(10)-triene-3, 17β-diol. The structural formula is: C 18 H 24 O 2 M.W. 272.38 Inactive Ingredients: Colloidal silicon dioxide, corn starch, microcrystalline cellulose, lactose monohydrate, magnesium stearate, and sodium starch glycolate. In addition, the 1 mg also contains FD&C blue no. 1 aluminum lake and D&C red no. 27 aluminum lake. The 2 mg also contains FD&C blue no. 1 aluminum lake and D&C yellow no. 10 aluminum lake. FDA approved dissolution test specifications differ from USP. structure

Estradiol ESTRADIOL

ESTRADIOL 42.5 g

TEVA PHARMACEUTICALS USA, INC. FDA Rx Only

Each gram of estradiol vaginal cream, USP, 0.01% contains 0.1 mg estradiol in a nonliquefying base containing purified water, propylene glycol, stearyl alcohol, white ceresin wax, mono- and di-glycerides, hypromellose 2208 (4000 cps), sodium lauryl sulfate, methylparaben, edetate di-sodium and tertiary -butylhydroquinone. Estradiol is chemically described as estra-1,3,5(10)-triene-3, 17(beta)-diol. It has an empirical formula of C18H24O2 and molecular weight of 272.37. The structural formula is: structural formula

3.6oz BiEST 2.5 Estrogen Cream ESTRIOLESTRADIOLESTROGEN

3.6OZ BIEST 2.5 ESTROGEN CREAM (ESTRIOLESTRADIO...) 2 %

SHYNE BRANDS/BIOLABS PRO FDA OTC

USES: This is a topical cream that contains bio-identical estriol and estradiol derived from wild yam and formulated in an 80:20 ratio. When applied to the skin it can help balance your hormones and provide temporary relief from menopausal symptoms such as hot flashes. DIRECTIONS: Apply once or twice a day. Massage into inner arms, thighs, chest or apply to inner forearm and rub arms together or use as directed by your Physician.

ABIGALE LO, ABIGALE ESTRADIOL AND NORETHINDRONE ACETATE

ABIGALE LO (ESTRADIOL AND N...) 1 mg/0.5 mg Tablet

XIROMED LLC FDA Rx Only

Abigale, 1 mg/0.5 mg is a single tablet for oral administration containing 1 mg of estradiol and 0.5 mg of norethindrone acetate and the following excipients: maize starch, lactose monohydrate, FD&C Yellow No. 6, copovidone, talc and magnesium stearate. Abigale Lo, 0.5 mg/0.1 mg is a single tablet for oral administration containing 0.5 mg of estradiol and 0.1 mg of norethindrone acetate and the following excipients: maize starch, lactose monohydrate, FD&C Yellow No. 6, copovidone, talc and magnesium stearate. Estradiol (E 2 ), is a white or almost white crystalline powder. Its chemical name is estra-1, 3, 5 (10)-triene-3, 17β-diol hemihydrate with the empirical formula of C 18 H 24 O 2 , ½ H 2 O and a molecular weight of 281.4. The structural formula of E 2 is as follows: Norethindrone acetate (NETA) is a white or yellowish-white crystalline powder. Its chemical name is 17β -acetoxy-19-nor-17α -pregn-4-en-20-yn-3-one with the empirical formula of C 22 H 28 O 3 and molecular weight of 340.5. The structural formula of NETA is as follows: Estradiol Structural Formula Norethindrone Acetate Structural Formula

Activella ESTRADIOL NORETHINDRONE ACETATE

ACTIVELLA (ESTRADIOL NORET...) 1 mg/0.5 mg Tablet

AMNEAL PHARMACEUTICALS LLC FDA Rx Only

Activella 1 mg/0.5 mg is a single tablet for oral administration containing 1 mg of estradiol and 0.5 mg of norethindrone acetate and the following excipients: lactose monohydrate, starch (corn), copovidone, talc, magnesium stearate, hypromellose and triacetin. Activella 0.5 mg/0.1 mg is a single tablet for oral administration containing 0.5 mg of estradiol and 0.1 mg of norethindrone acetate and the following excipients: lactose monohydrate, starch (corn), hydroxypropylcellulose, talc, magnesium stearate, hypromellose and triacetin. Estradiol is a white or almost white crystalline powder. Its chemical name is estra-1, 3, 5 (10)-triene-3, 17β-diol hemihydrate with the empirical formula of C 18 H 24 O 2 ,1/2; H 2 O and a molecular weight of 281.4. The structural formula of E 2 is as follows: Estradiol Norethindrone acetate (NETA) is a white or yellowish-white crystalline powder. Its chemical name is 17β-acetoxy-19-nor-17α-pregn-4-en-20-yn-3-one with the empirical formula of C 22 H 28 O 3 and molecular weight of 340.5. The structural formula of NETA is as follows: Norethindrone Acetate Estradiol structural formula Norethindrone Acetate structural formula

Angeliq DROSPIRENONE AND ESTRADIOL

ANGELIQ (DROSPIRENONE AN...) 0.25 mg Tablet

BAYER HEALTHCARE PHARMACEUTICALS INC. FDA Rx Only

Angeliq tablets, for oral administration, provide a hormone regimen consisting of drospirenone and estradiol. Drospirenone, (6R,7R,8R,9S,10R,13S,14S,15S,16S,17S)-1,3´,4´,6, 6a,7,8,9,10,11,12,13,14,15,15a,16-hexadecahydro-10,13-dimethylspiro-[17H-dicyclopropa[6,7:15,16]cyclopenta[a]phenanthrene- 17,2´(5H)-furan]-3,5´(2H)-dione (CAS) is a synthetic progestational compound and has a molecular weight of 366.5 and a molecular formula of C 24 H 30 O 3 . Estradiol USP, (Estra-1,3,5(10)-triene-3,17-diol,17ß), has a molecular weight of 272.39 and the molecular formula is C 18 H 24 O 2 . The structural formulas are as follows: The inactive ingredients in Angeliq 0.5 mg DRSP/1 mg E2 tablets are: lactose monohydrate NF, corn starch NF, pregelatinized starch NF, povidone 25000 USP, magnesium stearate NF, hydroxylpropylmethyl cellulose USP, macrogol 6000 NF, talc USP, titanium dioxide USP, and red ferric oxide pigment NF. The inactive ingredients in Angeliq 0.25 mg DRSP/0.5 mg E2 tablets are: lactose monohydrate NF, corn starch NF, pregelatinized starch NF, povidone 25000 USP, magnesium stearate NF, hydroxylpropylmethyl cellulose USP, macrogol 6000 NF, talc USP, titanium dioxide USP, and yellow ferric oxide pigment NF. Chemical Structure

Balance Plus Cream ESTRIOLESTRADIOLPROGESTERONEDHEA

BALANCE PLUS CREAM (ESTRIOLESTRADIO...) 6 %

SHYNE BRANDS/BIOLABS PRO FDA OTC

DIRECTIONS: Apply once or twice a day. Massage into inner arms, thighs, chest or apply to inner forearm and rub arms together or use as directed by your Physician.

BiEST 5.0 Estrogen Cream ESTRIOLESTRADIOL

BIEST 5.0 ESTROGEN CREAM (ESTRIOLESTRADIO...) 4 %

SHYNE BRANDS FDA OTC

USES: This is a topical cream that contains bio-identical estriol and estradiol derived from wild yam and formulated in an 80:20 ratio. When applied to the skin it can help balance your hormones and provide temporary relief from menopausal symptoms such as hot flashes. DIRECTIONS: Apply once or twice a day. Massage into inner arms, thighs, chest or apply to inner forearm and rub arms together or use as directed by your Physician.

BiEST 5.0 Estrogen Cream - 3.6oz ESTRIOLESTRADIOL

BIEST 5.0 ESTROGEN CREAM - 3.6OZ (ESTRIOLESTRADIO...) 4 %

SHYNE BRANDS/BIOLABS PRO FDA OTC

USES: This is a topical cream that contains bio-identical estriol and estradiol derived from wild yam and formulated in an 80:20 ratio. When applied to the skin it can help balance your hormones and provide temporary relief from menopausal symptoms such as hot flashes. DIRECTIONS: Apply once or twice a day. Massage into inner arms, thighs, chest or apply to inner forearm and rub arms together or use as directed by your Physician.

Bijuva ESTRADIOL AND PROGESTERONE

BIJUVA (ESTRADIOL AND P...) 0.5 mg/100 mg Capsule

MAYNE PHARMA LLC FDA Rx Only

BIJUVA (estradiol and progesterone) is an oval shaped opaque capsule in which the estradiol is solubilized and the progesterone is micronized and suspended in the mixture of medium chain mono and di-glycerides and lauroyl polyoxyl-32 glycerides. Each 0.5 mg/100 mg capsule is light pink on one side, dark pink on the other side, and printed with "5C1" in white ink. Each 1 mg/100 mg capsule is light pink on one side, dark pink on the other side, and printed with "1C1" in white ink. Estradiol (estra-1,3,5 (10)-triene-3,17β-diol), an estrogen, has a molecular weight of 272.38, and chemical formula C 18 H 24 O 2 . Progesterone (pregn-4-ene-3, 20-dione) has a molecular weight of 314.47, and chemical formula C 21 H 30 O 2 . The structural formulas are as follows: Estradiol Progesterone Each BIJUVA (estradiol and progesterone) capsule contains the following inactive ingredients: ammonium hydroxide, ethanol, ethyl acetate, FD&C Red #40, gelatin, glycerin, hydrolyzed gelatin, isopropyl alcohol, lauroyl polyoxyl-32 glycerides, lecithin, medium chain mono and di-glycerides, medium chain triglycerides, polyethylene glycol, polyvinyl acetate phthalate, propylene glycol, purified water, and titanium dioxide. Structural Formula Structural Formula

Bijuva ESTRADIOL AND PROGESTERONE

BIJUVA (ESTRADIOL AND P...) 0.5 mg/100 mg Capsule

MAYNE PHARMA FDA Rx Only

BIJUVA (estradiol and progesterone) is an oval shaped opaque capsule in which the estradiol is solubilized and the progesterone is micronized and suspended in the mixture of medium chain mono and di-glycerides and lauroyl polyoxyl-32 glycerides. Each 0.5 mg/100 mg capsule is light pink on one side, dark pink on the other side, and printed with "5C1" in white ink. Each 1 mg/100 mg capsule is light pink on one side, dark pink on the other side, and printed with "1C1" in white ink. Estradiol (estra-1,3,5 (10)-triene-3,17β-diol), an estrogen, has a molecular weight of 272.38, and chemical formula C 18 H 24 O 2 . Progesterone (pregn-4-ene-3, 20-dione) has a molecular weight of 314.47, and chemical formula C 21 H 30 O 2 . The structural formulas are as follows: Estradiol Progesterone Each BIJUVA (estradiol and progesterone) capsule contains the following inactive ingredients: ammonium hydroxide, ethanol, ethyl acetate, FD&C Red #40, gelatin, glycerin, hydrolyzed gelatin, isopropyl alcohol, lauroyl polyoxyl-32 glycerides, lecithin, medium chain mono and di- glycerides, medium chain triglycerides, polyethylene glycol, polyvinyl acetate phthalate, propylene glycol, purified water, and titanium dioxide. Chemical Structure Chemical Structure

Climara ESTRADIOL

CLIMARA (ESTRADIOL) 0.025 mg

BAYER HEALTHCARE PHARMACEUTICALS INC. FDA Rx Only

Climara (estradiol transdermal system), is designed to release estradiol continuously upon application to intact skin. Six (6.5, 9.375, 12.5, 15, 18.75 and 25 cm 2 ) systems are available to provide nominal in vivo delivery of 0.025, 0.0375, 0.05, 0.06, 0.075 or 0.1 mg respectively of estradiol per day. The period of use is 7 days. Each system has a contact surface area of either 6.5, 9.375, 12.5, 15, 18.75 or 25 cm 2 , and contains 2, 2.85, 3.8, 4.55, 5.7 or 7.6 mg of estradiol USP respectively. The composition of the systems per unit area is identical. Estradiol USP is a white, crystalline powder, chemically described as estra-1,3,5(10)-triene-3, 17β-diol. It has an empirical formula of C 18 H 24 O 2 and molecular weight of 272.38. The structural formula is: The Climara transdermal system comprises three layers. Proceeding from the visible surface toward the surface attached to the skin, these layers are: 1. A translucent polyethylene film. 2. An acrylate adhesive matrix containing estradiol USP. 3. A protective liner of siliconized or fluoropolymer-coated polyester film is attached to the adhesive surface and must be removed before the system can be used. The active component of the transdermal system is estradiol. The remaining components of the transdermal system (acrylate copolymer adhesive, fatty acid esters, and polyethylene backing) are pharmacologically inactive. Chemical Structure Patch Diagram

Climara Pro ESTRADIOL AND LEVONORGESTREL

CLIMARA PRO (ESTRADIOL AND L...) 0.045 mg

BAYER HEALTHCARE PHARMACEUTICALS INC. FDA Rx Only

Climara Pro (estradiol/levonorgestrel transdermal system) is an adhesive-based matrix transdermal patch designed to release both estradiol and levonorgestrel, a progestational agent, continuously upon application to intact skin. The 22 cm 2 Climara Pro system contains 4.4 mg estradiol and 1.39 mg levonorgestrel and provides a nominal delivery rate (mg per day) of 0.045 estradiol and 0.015 levonorgestrel. Estradiol USP has a molecular weight of 272.39 and the molecular formula is C 18 H 24 O 2 . Levonorgestrel USP has a molecular weight of 312.4 and a molecular formula of C 21 H 28 O 2 . The structural formulas for estradiol and levonorgestrel are: The Climara Pro transdermal system comprises 3 layers. Proceeding from the visible surface towards the surface attached to the skin, these layers are: 1. A translucent polyethylene backing film. 2. An acrylate adhesive matrix containing estradiol and levonorgestrel. 3. A protective liner of either siliconized or fluoropolymer coated polyester film. The protective liner is attached to the adhesive surface and must be removed before the system can be used. The active components of the transdermal system are estradiol and levonorgestrel. The remaining components of the transdermal system (acrylate copolymer adhesive and polyvinylpyrrolidone/vinyl acetate copolymer) are pharmacologically inactive. Chemical structure diagram patch

CombiPatch (estradiol/norethindrone acetate transdermal system) ESTRADIOL NORETHINDRONE ACETATE TRANSDERMAL SYSTEM

COMBIPATCH (ESTRADIOL/NORETHINDRONE ACETATE TRANSDERMAL SYSTEM) (ESTRADIOL NORET...) 0.14 mg

NOVEN THERAPEUTICS, LLC FDA Rx Only

CombiPatch ® (estradiol/norethindrone acetate transdermal system) is an adhesive-based matrix transdermal patch designed to release both estradiol, an estrogen, and norethindrone acetate (NETA), a progestational agent, continuously upon application to intact skin. Two systems are available, providing the following in vivo delivery rates of estradiol and NETA. 1 NETA=norethindrone acetate. 2 Based on in vivo/in vitro flux data, delivery of both components per day via skin of average permeability (interindividual variation in skin permeability is approximately 20 percent). System Size Estradiol (mg) NETA 1 (mg) Nominal Delivery Rate 2 (mg per day) Estradiol / NETA 9 cm 2 round 0.62 2.7 0.05/0.14 16 cm 2 round 0.51 4.8 0.05/0.25 Estradiol USP (estradiol) is a white to creamy white, odorless, crystalline powder, chemically described as estra-1,3,5(10)-triene-3,17 β -diol. The molecular weight of estradiol is 272.39 and the molecular formula is C 18 H 24 O 2 . NETA USP is a white to creamy white, odorless, crystalline powder, chemically described as 17-hydroxy-19-nor-17α-pregn-4-en-20-yn-3-one acetate. The molecular weight of NETA is 340.47 and the molecular formula is C 22 H 28 O 3 . The structural formulas for estradiol and NETA are: CombiPatch is comprised of 3 layers. Proceeding from the visible surface toward the surface attached to the skin, these layers are (1) a translucent polyolefin film backing, (2) an adhesive layer containing estradiol, NETA, acrylic adhesive, silicone adhesive, oleic acid NF, povidone USP and dipropylene glycol, and (3) a polyester release protective liner, which is attached to the adhesive surface and must be removed before the system can be used. The active components of the system are estradiol USP and NETA USP. The remaining components of the system are pharmacologically inactive. Chemical Structure Layer

DIVIGEL ESTRADIOL

DIVIGEL (ESTRADIOL) 1.25 g Gel

VERTICAL PHARMACEUTICALS, LLC FDA Rx Only

Divigel (estradiol gel) 0.1 percent, is a clear, colorless gel, which is odorless when dry. It is designed to deliver sustained circulating concentrations of estradiol when applied once daily to the skin. The gel is applied to a small area (200 cm 2 ) of the thigh in a thin layer. Divigel is available in five doses of 0.25, 0.5, 0.75, 1.0, and 1.25 grams for topical application (corresponding to 0.25, 0.5, 0.75, 1.0, and 1.25 mg estradiol, respectively). The active component of the topical gel is estradiol. Estradiol is a white crystalline powder, chemically described as estra-1,3,5(10)-triene-3,17ß-diol. It has an empirical formula of C 18 H 24 O 2 and molecular weight of 272.39. The structural formula is: Divigel Chemical Structure The remaining components of the gel (carbomer, ethanol, propylene glycol, purified water, and triethanolamine) are pharmacologically inactive. Divigel Chemical Structure

DOTTI ESTRADIOL

DOTTI (ESTRADIOL) 0.025 mg

AMNEAL PHARMACEUTICALS LLC FDA Rx Only

DOTTI (estradiol transdermal system, USP) contains estradiol, USP in a multipolymeric adhesive. The system is designed to release estradiol, USP continuously upon application to intact skin. Five dosage strengths of DOTTI are available to provide nominal in vivo delivery rates of 0.025, 0.0375, 0.05, 0.075, or 0.1 mg of estradiol, USP per day via the skin. Each corresponding system has an active surface area of 1.89, 2.83, 3.78, 5.66, or 7.55 cm 2 and contains 0.314, 0.470, 0.627, 0.940, or 1.253 mg of estradiol USP, respectively. The composition of the systems per unit area is identical. Estradiol, USP is a white to practically white powder, chemically described as estra-1,3,5 (10)- triene-3,17β-diol. The structural formula is: The molecular formula of estradiol, USP is C 18 H 24 0 2 . The molecular weight is 272.39 g/mol. DOTTI is comprised of 3 layers. Proceeding from the visible surface toward the surface attached to the skin, these layers are (1) polyester and ethylene vinyl acetate copolymer film (2) an adhesive formulation containing estradiol USP, acrylic adhesive, silicone adhesive, oleyl alcohol, NF, povidone, USP and dipropylene glycol, and (3) a polyester release liner which is attached to the adhesive surface and must be removed before the system can be used. The active component of the system is estradiol, USP. The remaining components of the system are pharmacologically inactive. FDA approved acceptance criteria for dissolution test specifications differ from USP. 1 2

DOTTI ESTRADIOL

DOTTI (ESTRADIOL) 0.025 mg

BRYANT RANCH PREPACK FDA Rx Only

DOTTI (estradiol transdermal system, USP) contains estradiol, USP in a multipolymeric adhesive. The system is designed to release estradiol, USP continuously upon application to intact skin. Five dosage strengths of DOTTI are available to provide nominal in vivo delivery rates of 0.025, 0.0375, 0.05, 0.075, or 0.1 mg of estradiol, USP per day via the skin. Each corresponding system has an active surface area of 1.89, 2.83, 3.78, 5.66, or 7.55 cm 2 and contains 0.314, 0.470, 0.627, 0.940, or 1.253 mg of estradiol USP, respectively. The composition of the systems per unit area is identical. Estradiol, USP is a white to practically white powder, chemically described as estra-1,3,5 (10)- triene-3,17β-diol. The structural formula is: The molecular formula of estradiol, USP is C 18 H 24 0 2 . The molecular weight is 272.39 g/mol. DOTTI is comprised of 3 layers. Proceeding from the visible surface toward the surface attached to the skin, these layers are (1) polyester and ethylene vinyl acetate copolymer film (2) an adhesive formulation containing estradiol USP, acrylic adhesive, silicone adhesive, oleyl alcohol, NF, povidone, USP and dipropylene glycol, and (3) a polyester release liner which is attached to the adhesive surface and must be removed before the system can be used. The active component of the system is estradiol, USP. The remaining components of the system are pharmacologically inactive. FDA approved acceptance criteria for dissolution test specifications differ from USP.

DOTTI ESTRADIOL

DOTTI (ESTRADIOL) 0.025 mg

BRYANT RANCH PREPACK FDA Rx Only

DOTTI (estradiol transdermal system, USP) contains estradiol, USP in a multipolymeric adhesive. The system is designed to release estradiol, USP continuously upon application to intact skin. Five dosage strengths of DOTTI are available to provide nominal in vivo delivery rates of 0.025, 0.0375, 0.05, 0.075, or 0.1 mg of estradiol, USP per day via the skin. Each corresponding system has an active surface area of 1.89, 2.83, 3.78, 5.66, or 7.55 cm 2 and contains 0.314, 0.470, 0.627, 0.940, or 1.253 mg of estradiol USP, respectively. The composition of the systems per unit area is identical. Estradiol, USP is a white to practically white powder, chemically described as estra-1,3,5 (10)- triene-3,17β-diol. The structural formula is: The molecular formula of estradiol, USP is C 18 H 24 0 2 . The molecular weight is 272.39 g/mol. DOTTI is comprised of 3 layers. Proceeding from the visible surface toward the surface attached to the skin, these layers are (1) polyester and ethylene vinyl acetate copolymer film (2) an adhesive formulation containing estradiol USP, acrylic adhesive, silicone adhesive, oleyl alcohol, NF, povidone, USP and dipropylene glycol, and (3) a polyester release liner which is attached to the adhesive surface and must be removed before the system can be used. The active component of the system is estradiol, USP. The remaining components of the system are pharmacologically inactive. FDA approved acceptance criteria for dissolution test specifications differ from USP.

DOTTI ESTRADIOL

DOTTI (ESTRADIOL) 0.025 mg

BRYANT RANCH PREPACK FDA Rx Only

DOTTI (estradiol transdermal system, USP) contains estradiol, USP in a multipolymeric adhesive. The system is designed to release estradiol, USP continuously upon application to intact skin. Five dosage strengths of DOTTI are available to provide nominal in vivo delivery rates of 0.025, 0.0375, 0.05, 0.075, or 0.1 mg of estradiol, USP per day via the skin. Each corresponding system has an active surface area of 1.89, 2.83, 3.78, 5.66, or 7.55 cm 2 and contains 0.314, 0.470, 0.627, 0.940, or 1.253 mg of estradiol USP, respectively. The composition of the systems per unit area is identical. Estradiol, USP is a white to practically white powder, chemically described as estra-1,3,5 (10)- triene-3,17β-diol. The structural formula is: The molecular formula of estradiol, USP is C 18 H 24 0 2 . The molecular weight is 272.39 g/mol. DOTTI is comprised of 3 layers. Proceeding from the visible surface toward the surface attached to the skin, these layers are (1) polyester and ethylene vinyl acetate copolymer film (2) an adhesive formulation containing estradiol USP, acrylic adhesive, silicone adhesive, oleyl alcohol, NF, povidone, USP and dipropylene glycol, and (3) a polyester release liner which is attached to the adhesive surface and must be removed before the system can be used. The active component of the system is estradiol, USP. The remaining components of the system are pharmacologically inactive. FDA approved acceptance criteria for dissolution test specifications differ from USP.

DOTTI ESTRADIOL

DOTTI (ESTRADIOL) 0.025 mg

BRYANT RANCH PREPACK FDA Rx Only

DOTTI (estradiol transdermal system, USP) contains estradiol, USP in a multipolymeric adhesive. The system is designed to release estradiol, USP continuously upon application to intact skin. Five dosage strengths of DOTTI are available to provide nominal in vivo delivery rates of 0.025, 0.0375, 0.05, 0.075, or 0.1 mg of estradiol, USP per day via the skin. Each corresponding system has an active surface area of 1.89, 2.83, 3.78, 5.66, or 7.55 cm 2 and contains 0.314, 0.470, 0.627, 0.940, or 1.253 mg of estradiol USP, respectively. The composition of the systems per unit area is identical. Estradiol, USP is a white to practically white powder, chemically described as estra-1,3,5 (10)- triene-3,17β-diol. The structural formula is: The molecular formula of estradiol, USP is C 18 H 24 0 2 . The molecular weight is 272.39 g/mol. DOTTI is comprised of 3 layers. Proceeding from the visible surface toward the surface attached to the skin, these layers are (1) polyester and ethylene vinyl acetate copolymer film (2) an adhesive formulation containing estradiol USP, acrylic adhesive, silicone adhesive, oleyl alcohol, NF, povidone, USP and dipropylene glycol, and (3) a polyester release liner which is attached to the adhesive surface and must be removed before the system can be used. The active component of the system is estradiol, USP. The remaining components of the system are pharmacologically inactive. FDA approved acceptance criteria for dissolution test specifications differ from USP.

DOTTI ESTRADIOL

DOTTI (ESTRADIOL) 0.025 mg

BRYANT RANCH PREPACK FDA Rx Only

DOTTI (estradiol transdermal system, USP) contains estradiol, USP in a multipolymeric adhesive. The system is designed to release estradiol, USP continuously upon application to intact skin. Five dosage strengths of DOTTI are available to provide nominal in vivo delivery rates of 0.025, 0.0375, 0.05, 0.075, or 0.1 mg of estradiol, USP per day via the skin. Each corresponding system has an active surface area of 1.89, 2.83, 3.78, 5.66, or 7.55 cm 2 and contains 0.314, 0.470, 0.627, 0.940, or 1.253 mg of estradiol USP, respectively. The composition of the systems per unit area is identical. Estradiol, USP is a white to practically white powder, chemically described as estra-1,3,5 (10)- triene-3,17β-diol. The structural formula is: The molecular formula of estradiol, USP is C 18 H 24 0 2 . The molecular weight is 272.39 g/mol. DOTTI is comprised of 3 layers. Proceeding from the visible surface toward the surface attached to the skin, these layers are (1) polyester and ethylene vinyl acetate copolymer film (2) an adhesive formulation containing estradiol USP, acrylic adhesive, silicone adhesive, oleyl alcohol, NF, povidone, USP and dipropylene glycol, and (3) a polyester release liner which is attached to the adhesive surface and must be removed before the system can be used. The active component of the system is estradiol, USP. The remaining components of the system are pharmacologically inactive. FDA approved acceptance criteria for dissolution test specifications differ from USP.

Dr Dale Wellness NU Fem 1 2 3 All In One Topical Homeopathic DHEAADRENAL CORTISOLGLANDULA SUPRARENALIS SUISHUMAN GROWTH HORMONEIGF IIGF II HYPOTHALAMUSPITUITARYPLACENTALIVERTHYMUSRNADNAESTROGENIUMESTRADIOLINUMSANGUINARA CANDENSISOOPHORINUMPROGESTERONIUMPITITUARINUMPINEALFOLLICULINUMOVARINUMCHELADONIUMSULPHURSEPIALAGENINE TESTOSTERONECIMICIFUGA BLACK COHOSHLILIUM TIGRINUMGRAPHITESKALI PHOSPHORICUM CAUSTICUMCALCAREA CARBONICAPHYTOLACCASCROPHULARIA NODOSA

DR DALE WELLNESS NU FEM 1 2 3 ALL IN ONE TOPICAL HOMEOPATHIC (DHEAADRENAL COR...)

DMD CLINICAL NATUROPATHY FDA OTC

Uses Topical gel, applied to skin

GABA GABA .GAMMA.-AMINOBUTYRIC ACID .GAMMA.-AMINOBUTYRIC ACID WATER ALCOHOL

OTC Limited

HOMEOPATHIC INDICATIONS: For temporary relief of symptoms including anger, hostility, sleep difficulties and fatigue.** **These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

RENEWAL HGH ADVANCED RNA, Silicea, Phosphoricum Acidum, Pituitaria Glandula (Suis), Sulphur, Zincum Sulphuricum, HGH, Selenium Metallicum, Colostrum (Human) SACCHAROMYCES CEREVISIAE RNA SACCHAROMYCES CEREVISIAE RNA SILICON DIOXIDE SILICON DIOXIDE PHOSPHORIC ACID PHOSPHORIC ACID SUS SCROFA PITUITARY GLAND, POSTERIOR SUS SCROFA PITUITARY GLAND, POSTERIOR SULFUR SULFUR ZINC SULFATE HEPTAHYDRATE ZINC CATION SOMATROPIN SOMATROPIN SELENIUM SELENIUM HUMAN COLOSTRUM COLOSTRUM HUMAN WATER GLYCERIN ALCOHOL

OTC Limited

INDICATIONS: To temporarily relieve symptoms related to aging; tiredness, weakness, excess fat, wrinkled skin, lack of muscle, etc.

Lipotox Squalene, Cholesterinum, Estradiol, Progesterone, Aspartame, Benzalkonium Chloride, Formalinum, Methylene Chloride, Methyl Paraben, Propyl Paraben, Sodium Benzoate, Sodium Citrate, Titanium Dioxide, Zincum Oxydatum, Arsenicum Album, Lycopodium Clavatum, Nux Vomica, Phosphoricum Acidum, Phosphorus, Aceticum Acidum, Adrenocorticotrophin, Benzoicum Acidum, Benzyl Alcohol, Boricum Acidum, Chlorinum, Cortisone Aceticum, Eugenol, Folliculinum, Isopropyl Palmitate, Lacticum Acidum, Petroleum Jelly SQUALENE SQUALENE CHOLESTEROL CHOLESTEROL ESTRADIOL ESTRADIOL PROGESTERONE PROGESTERONE ASPARTAME ASPARTAME BENZALKONIUM CHLORIDE BENZALKONIUM FORMALDEHYDE FORMALDEHYDE METHYLENE CHLORIDE METHYLENE CHLORIDE METHYLPARABEN METHYLPARABEN PROPYLPARABEN PROPYLPARABEN SODIUM BENZOATE BENZOIC ACID ANHYDROUS TRISODIUM CITRATE ANHYDROUS CITRIC ACID TITANIUM DIOXIDE TITANIUM DIOXIDE ZINC OXIDE ZINC CATION ARSENIC TRIOXIDE ARSENIC CATION (3+) LYCOPODIUM CLAVATUM SPORE LYCOPODIUM CLAVATUM SPORE STRYCHNOS NUX-VOMICA SEED STRYCHNOS NUX-VOMICA SEED PHOSPHORIC ACID PHOSPHORIC ACID PHOSPHORUS PHOSPHORUS ACETIC ACID ACETIC ACID CORTICOTROPIN CORTICOTROPIN BENZOIC ACID BENZOIC ACID BENZYL ALCOHOL BENZYL ALCOHOL BORIC ACID BORIC ACID CHLORINE CHLORINE CORTISONE ACETATE CORTISONE EUGENOL EUGENOL ESTRONE ESTRONE ISOPROPYL ALCOHOL ISOPROPYL ALCOHOL LACTIC ACID, DL- LACTIC ACID, DL- PETROLATUM PETROLATUM PHENYLBUTAZONE PHENYLBUTAZONE LEAD LEAD POTASSIUM SORBATE SORBIC ACID RESORCINOL RESORCINOL SALICYLIC ACID SALICYLIC ACID SORBITOL SORBITOL STEARYL ALCOHOL STEARYL ALCOHOL XYLITOL XYLITOL WATER ALCOHOL CASTOR OIL BORAGE OIL

OTC Limited

INDICATIONS: For temporary relief of exhaustion & restlessness, metallic taste & dyspepsia & menstrual pain.

Matrix Support Ceanothus Americanus, Anacardium Orientale, Argentum Nitricum, Condurango, Hydrastis Canadensis, Momordica Balsamina, Oxalis Acetosella, Pulsatilla (Vulgaris), Bile Duct (Suis), Colon (Suis), Duodenum (Suis), Esophagus (Suis), Eye (Suis), Gallbladder (Suis), Ileum (Suis), Intestine (Suis), Ipecacuanha, Jejunum (Suis), Kali Bichromicum, Lung (Suis), Mucosa Nasalis Suis, Natrum Oxalaceticum, Oral Mucosa (Suis), Pancreas Suis, Phosphorus, Rectal Mucosa (Suis), Stomach (Suis), Sulphur, Veratrum Album, Mannan, CEANOTHUS AMERICANUS LEAF CEANOTHUS AMERICANUS LEAF SEMECARPUS ANACARDIUM JUICE SEMECARPUS ANACARDIUM JUICE SILVER NITRATE SILVER CATION MARSDENIA CONDURANGO BARK MARSDENIA CONDURANGO BARK GOLDENSEAL GOLDENSEAL MOMORDICA BALSAMINA IMMATURE FRUIT MOMORDICA BALSAMINA IMMATURE FRUIT OXALIS ACETOSELLA LEAF OXALIS ACETOSELLA LEAF PULSATILLA VULGARIS ANEMONE PULSATILLA SUS SCROFA BILE DUCT SUS SCROFA BILE DUCT SUS SCROFA COLON SUS SCROFA COLON SUS SCROFA DUODENUM SUS SCROFA DUODENUM SUS SCROFA ESOPHAGUS SUS SCROFA ESOPHAGUS SUS SCROFA EYE SUS SCROFA EYE SUS SCROFA GALLBLADDER SUS SCROFA GALLBLADDER SUS SCROFA ILEUM SUS SCROFA ILEUM PORK INTESTINE PORK INTESTINE IPECAC IPECAC SUS SCROFA JEJUNUM SUS SCROFA JEJUNUM POTASSIUM DICHROMATE DICHROMATE ION SUS SCROFA LUNG SUS SCROFA LUNG SUS SCROFA NASAL MUCOSA SUS SCROFA NASAL MUCOSA SODIUM DIETHYL OXALACETATE DIETHYL OXALACETATE SUS SCROFA ORAL MUCOSA SUS SCROFA ORAL MUCOSA SUS SCROFA PANCREAS SUS SCROFA PANCREAS PHOSPHORUS PHOSPHORUS SUS SCROFA RECTAL MUCOSA SUS SCROFA RECTAL MUCOSA SUS SCROFA STOMACH SUS SCROFA STOMACH SULFUR SULFUR VERATRUM ALBUM ROOT VERATRUM ALBUM ROOT YEAST MANNAN YEAST MANNAN WOOD CREOSOTE WOOD CREOSOTE LACHESIS MUTA VENOM LACHESIS MUTA VENOM MANDRAGORA OFFICINARUM ROOT MANDRAGORA OFFICINARUM ROOT SUS SCROFA URINARY BLADDER SUS SCROFA URINARY BLADDER SHIGELLA DYSENTERIAE SHIGELLA DYSENTERIAE WATER ALCOHOL

OTC Limited

HOMEOPATHIC INDICATIONS: For the temporary relief of symptoms such as occasional diarrhea, occasional constipation, headaches, gas, congestion, irritated eyes, and indigestion.** **These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.

LYM D Chelidonium Majus, Echinacea (Angustifolia), Nasturtium Aquaticum, Taraxacum Officinale, Trifolium Pratense, Urtica Dioica, Hydrastis Canadensis, Thymus (Suis), Thyroidinum (Suis), Arsenicum Album, Coccus Cacti, Lycopodium Clavatum, Phosphorus, Rhus Tox, Borrelia Burgdorferi Nosode, Ledum Palustre CHELIDONIUM MAJUS CHELIDONIUM MAJUS ECHINACEA ANGUSTIFOLIA ECHINACEA ANGUSTIFOLIA NASTURTIUM OFFICINALE NASTURTIUM OFFICINALE TARAXACUM OFFICINALE TARAXACUM OFFICINALE TRIFOLIUM PRATENSE FLOWER TRIFOLIUM PRATENSE FLOWER URTICA DIOICA URTICA DIOICA GOLDENSEAL GOLDENSEAL SUS SCROFA THYMUS SUS SCROFA THYMUS SUS SCROFA THYROID SUS SCROFA THYROID ARSENIC TRIOXIDE ARSENIC CATION (3+) PROTORTONIA CACTI PROTORTONIA CACTI LYCOPODIUM CLAVATUM SPORE LYCOPODIUM CLAVATUM SPORE PHOSPHORUS PHOSPHORUS TOXICODENDRON PUBESCENS LEAF TOXICODENDRON PUBESCENS LEAF BORRELIA BURGDORFERI BORRELIA BURGDORFERI LEDUM PALUSTRE TWIG LEDUM PALUSTRE TWIG WATER ALCOHOL

OTC Limited

INDICATIONS: For temporary relief of aches and pains of joints and muscles as a consequence of infection.

Texaclear homeopathic Allergy Releif plus cedar fever over 100 extracts trees,weeds and grasses BETULA NIGRA POLLEN BETULA NIGRA POLLEN JUNIPERUS PINCHOTII POLLEN JUNIPERUS PINCHOTII POLLEN POPULUS DELTOIDES SUBSP. MONILIFERA POLLEN POPULUS DELTOIDES SUBSP. MONILIFERA POLLEN MELALEUCA QUINQUENERVIA POLLEN MELALEUCA QUINQUENERVIA POLLEN QUERCUS GAMBELII POLLEN QUERCUS GAMBELII POLLEN THUJA OCCIDENTALIS LEAF THUJA OCCIDENTALIS LEAF PINUS PONDEROSA POLLEN PINUS PONDEROSA POLLEN JUNIPERUS SCOPULORUM POLLEN JUNIPERUS SCOPULORUM POLLEN AMBROSIA DUMOSA POLLEN AMBROSIA DUMOSA POLLEN QUERCUS VIRGINIANA POLLEN QUERCUS VIRGINIANA POLLEN PINUS NIGRA POLLEN PINUS NIGRA POLLEN LIQUIDAMBAR STYRACIFLUA POLLEN LIQUIDAMBAR STYRACIFLUA POLLEN AILANTHUS ALTISSIMA POLLEN AILANTHUS ALTISSIMA POLLEN QUERCUS ALBA WHOLE QUERCUS ALBA WHOLE FAGUS GRANDIFOLIA POLLEN FAGUS GRANDIFOLIA POLLEN CARYA GLABRA POLLEN CARYA GLABRA POLLEN IVA ANGUSTIFOLIA POLLEN IVA ANGUSTIFOLIA POLLEN PLANTAGO LANCEOLATA POLLEN PLANTAGO LANCEOLATA POLLEN QUERCUS VELUTINA WHOLE QUERCUS VELUTINA WHOLE RUMEX ACETOSELLA POLLEN RUMEX ACETOSELLA POLLEN ALNUS INCANA SUBSP. RUGOSA POLLEN ALNUS INCANA SUBSP. RUGOSA POLLEN ARTEMISIA VULGARIS WHOLE ARTEMISIA VULGARIS WHOLE CYCLACHAENA XANTHIFOLIA POLLEN CYCLACHAENA XANTHIFOLIA POLLEN FRAXINUS VELUTINA POLLEN FRAXINUS VELUTINA POLLEN JUNIPERUS ASHEI POLLEN JUNIPERUS ASHEI POLLEN JUNIPERUS VIRGINIANA POLLEN JUNIPERUS VIRGINIANA POLLEN POA PRATENSIS POLLEN POA PRATENSIS POLLEN FESTUCA PRATENSIS POLLEN FESTUCA PRATENSIS POLLEN PHALARIS ARUNDINACEA POLLEN PHALARIS ARUNDINACEA POLLEN PASPALUM NOTATUM POLLEN PASPALUM NOTATUM POLLEN CARYA ALBA POLLEN CARYA ALBA POLLEN SECALE CEREALE POLLEN SECALE CEREALE POLLEN ULMUS PUMILA POLLEN ULMUS PUMILA POLLEN CELTIS OCCIDENTALIS POLLEN CELTIS OCCIDENTALIS POLLEN MAGNESIUM STEARATE THUJA PLICATA LEAF THUJA PLICATA LEAF AMBROSIA ACANTHICARPA POLLEN AMBROSIA ACANTHICARPA POLLEN AMBROSIA ARTEMISIIFOLIA POLLEN AMBROSIA ARTEMISIIFOLIA POLLEN BAPTISIA TINCTORIA ROOT BAPTISIA TINCTORIA ROOT HYDRASTIS CANADENSIS WHOLE HYDRASTIS CANADENSIS WHOLE QUERCUS RUBRA BARK QUERCUS RUBRA BARK POPULUS NIGRA POLLEN POPULUS NIGRA POLLEN ELYMUS REPENS POLLEN ELYMUS REPENS POLLEN GUTIERREZIA SAROTHRAE WHOLE GUTIERREZIA SAROTHRAE WHOLE ARTEMISIA LUDOVICIANA WHOLE ARTEMISIA LUDOVICIANA WHOLE ARTEMISIA ANNUA POLLEN ARTEMISIA ANNUA POLLEN XANTHIUM STRUMARIUM POLLEN XANTHIUM STRUMARIUM POLLEN SOLIDAGO CANADENSIS WHOLE SOLIDAGO CANADENSIS WHOLE URTICA DIOICA POLLEN URTICA DIOICA POLLEN MICROCRYSTALLINE CELLULOSE FRAXINUS PENNSYLVANICA POLLEN FRAXINUS PENNSYLVANICA POLLEN POPULUS DELTOIDES SUBSP. DELTOIDES POLLEN POPULUS DELTOIDES SUBSP. DELTOIDES POLLEN CARYA CORDIFORMIS WHOLE CARYA CORDIFORMIS WHOLE CARYA OVATA POLLEN CARYA OVATA POLLEN CARYA LACINIOSA POLLEN CARYA LACINIOSA POLLEN AMBROSIA TRIFIDA POLLEN AMBROSIA TRIFIDA POLLEN BASSIA SCOPARIA POLLEN BASSIA SCOPARIA POLLEN AMARANTHUS HYBRIDUS POLLEN AMARANTHUS HYBRIDUS POLLEN CUPRESSUS ARIZONICA POLLEN CUPRESSUS ARIZONICA POLLEN TAXODIUM DISTICHUM POLLEN TAXODIUM DISTICHUM POLLEN JUNIPERUS MONOSPERMA POLLEN JUNIPERUS MONOSPERMA POLLEN BROUSSONETIA PAPYRIFERA POLLEN BROUSSONETIA PAPYRIFERA POLLEN PINUS SYLVESTRIS POLLEN PINUS SYLVESTRIS POLLEN AMARANTHUS PALMERI POLLEN AMARANTHUS PALMERI POLLEN AMBROSIA BIDENTATA POLLEN AMBROSIA BIDENTATA POLLEN AMBROSIA PSILOSTACHYA POLLEN AMBROSIA PSILOSTACHYA POLLEN CYNODON DACTYLON POLLEN CYNODON DACTYLON POLLEN ULMUS AMERICANA POLLEN ULMUS AMERICANA POLLEN ULMUS CRASSIFOLIA POLLEN ULMUS CRASSIFOLIA POLLEN JUNIPERUS OSTEOSPERMA POLLEN JUNIPERUS OSTEOSPERMA POLLEN IVA ANNUA POLLEN IVA ANNUA POLLEN JUNIPER BERRY JUNIPER BERRY ACER RUBRUM POLLEN ACER RUBRUM POLLEN PASCOPYRUM SMITHII POLLEN PASCOPYRUM SMITHII POLLEN FRAXINUS AMERICANA POLLEN FRAXINUS AMERICANA POLLEN DISTICHLIS SPICATA POLLEN DISTICHLIS SPICATA POLLEN HOLCUS LANATUS POLLEN HOLCUS LANATUS POLLEN ARTEMISIA TRIDENTATA POLLEN ARTEMISIA TRIDENTATA POLLEN CARPINUS CAROLINIANA WHOLE CARPINUS CAROLINIANA WHOLE RUMEX CRISPUS POLLEN RUMEX CRISPUS POLLEN AMARANTHUS SPINOSUS POLLEN AMARANTHUS SPINOSUS POLLEN ACER NEGUNDO POLLEN ACER NEGUNDO POLLEN ACACIA POLLEN ACACIA POLLEN POPULUS FREMONTII POLLEN POPULUS FREMONTII POLLEN AMBROSIA CONFERTIFLORA POLLEN AMBROSIA CONFERTIFLORA POLLEN CROSCARMELLOSE SODIUM SILICON DIOXIDE XYLITOL RORIPPA NASTURTIUM-AQUATICUM RORIPPA NASTURTIUM-AQUATICUM PHYTOLACCA AMERICANA ROOT PHYTOLACCA AMERICANA ROOT ECHINACEA, UNSPECIFIED ECHINACEA, UNSPECIFIED POA ANNUA POLLEN POA ANNUA POLLEN SORGHUM HALEPENSE POLLEN SORGHUM HALEPENSE POLLEN DACTYLIS GLOMERATA POLLEN DACTYLIS GLOMERATA POLLEN LOLIUM PERENNE POLLEN LOLIUM PERENNE POLLEN TRITICUM AESTIVUM POLLEN TRITICUM AESTIVUM POLLEN ZEA MAYS POLLEN ZEA MAYS POLLEN ANTHOXANTHUM ODORATUM POLLEN ANTHOXANTHUM ODORATUM POLLEN BACCHARIS HALIMIFOLIA WHOLE BACCHARIS HALIMIFOLIA WHOLE LIGUSTRUM LUCIDUM WHOLE LIGUSTRUM LUCIDUM WHOLE PINUS STROBUS POLLEN PINUS STROBUS POLLEN ATRIPLEX CANESCENS POLLEN ATRIPLEX CANESCENS POLLEN QUERCUS STELLATA POLLEN QUERCUS STELLATA POLLEN BETULA OCCIDENTALIS WHOLE BETULA OCCIDENTALIS WHOLE QUERCUS NIGRA POLLEN QUERCUS NIGRA POLLEN ACER SACCHARINUM POLLEN ACER SACCHARINUM POLLEN MORUS RUBRA POLLEN MORUS RUBRA POLLEN CARYA ILLINOINENSIS POLLEN CARYA ILLINOINENSIS POLLEN PINUS TAEDA POLLEN PINUS TAEDA POLLEN ALLENROLFEA OCCIDENTALIS POLLEN ALLENROLFEA OCCIDENTALIS POLLEN POPULUS ALBA POLLEN POPULUS ALBA POLLEN PLATANUS OCCIDENTALIS POLLEN PLATANUS OCCIDENTALIS POLLEN SALIX NIGRA POLLEN SALIX NIGRA POLLEN SORGHUM X DRUMMONDII WHOLE SORGHUM X DRUMMONDII WHOLE QUERCUS MACROCARPA POLLEN QUERCUS MACROCARPA POLLEN ULMUS CRASSIFOLIA WHOLE ULMUS CRASSIFOLIA WHOLE LOLIUM MULTIFLORUM POLLEN LOLIUM MULTIFLORUM POLLEN TAMARIX GALLICA POLLEN TAMARIX GALLICA POLLEN OSTRYA VIRGINIANA WHOLE OSTRYA VIRGINIANA WHOLE JUNIPERUS DEPPEANA WHOLE JUNIPERUS DEPPEANA WHOLE MORUS ALBA WHOLE MORUS ALBA WHOLE CEDRUS DEODARA WOOD CEDRUS DEODARA WOOD MYRRH MYRRH TRIGONELLA FOENUM-GRAECUM WHOLE TRIGONELLA FOENUM-GRAECUM WHOLE BETULA LENTA POLLEN BETULA LENTA POLLEN AGROSTIS GIGANTEA POLLEN AGROSTIS GIGANTEA POLLEN PHLEUM PRATENSE POLLEN PHLEUM PRATENSE POLLEN CHENOPODIUM ALBUM POLLEN CHENOPODIUM ALBUM POLLEN ALNUS RHOMBIFOLIA POLLEN ALNUS RHOMBIFOLIA POLLEN PINUS STROBUS BARK PINUS STROBUS BARK PROSOPIS PALLIDA POLLEN PROSOPIS PALLIDA POLLEN AMARANTHUS RETROFLEXUS POLLEN AMARANTHUS RETROFLEXUS POLLEN AVENA SATIVA POLLEN AVENA SATIVA POLLEN Embossed "TX" on upper and smooth on lower side tx

OTC Limited

this product is a homeopathic dilution,formulated to support the body's immunity for the temporary releif of allergies*

Lymphdrainex Geranium Robertianum, Nasturtium Aquaticum, Scrophularia Nodosa, Teucrium Scorodonia, Apis Mellifica, Equisetum Hyemale, Fumaria Officinalis, Natrum Sulphuricum, Phytolacca Decandra, Pinus Sylvestris, Veronica Officinalis, Aloe, Gentiana Lutea, Juglans Regia, Myosotis Arvensis, Sarsaparilla (Smilax Regelii), Baryta Carbonica, Hepar Sulphuris Calcareum, Mercurius Cyanatus, Ferrum Iodatum, Aranea Diadema, Calcarea Phosphorica, Parathyroid Gland (Bovine), Thymus (Suis), Thyroidinum (Suis) GERANIUM ROBERTIANUM GERANIUM ROBERTIANUM NASTURTIUM OFFICINALE NASTURTIUM OFFICINALE SCROPHULARIA NODOSA SCROPHULARIA NODOSA TEUCRIUM SCORODONIA FLOWERING TOP TEUCRIUM SCORODONIA FLOWERING TOP APIS MELLIFERA APIS MELLIFERA EQUISETUM HYEMALE EQUISETUM HYEMALE FUMARIA OFFICINALIS FLOWERING TOP FUMARIA OFFICINALIS FLOWERING TOP SODIUM SULFATE SODIUM SULFATE ANHYDROUS PHYTOLACCA AMERICANA ROOT PHYTOLACCA AMERICANA ROOT PINUS SYLVESTRIS LEAFY TWIG PINUS SYLVESTRIS LEAFY TWIG VERONICA OFFICINALIS FLOWERING TOP VERONICA OFFICINALIS FLOWERING TOP ALOE ALOE GENTIANA LUTEA ROOT GENTIANA LUTEA ROOT JUGLANS REGIA FRUIT RIND, IMMATURE JUGLANS REGIA FRUIT RIND, IMMATURE MYOSOTIS ARVENSIS MYOSOTIS ARVENSIS SMILAX ORNATA ROOT SMILAX ORNATA ROOT BARIUM CARBONATE BARIUM CATION CALCIUM SULFIDE CALCIUM SULFIDE MERCURIC CYANIDE MERCURIC CYANIDE FERROUS IODIDE FERROUS IODIDE ARANEUS DIADEMATUS ARANEUS DIADEMATUS TRIBASIC CALCIUM PHOSPHATE CALCIUM CATION BOS TAURUS PARATHYROID GLAND BOS TAURUS PARATHYROID GLAND SUS SCROFA THYMUS SUS SCROFA THYMUS SUS SCROFA THYROID SUS SCROFA THYROID WATER ALCOHOL

OTC Limited

INDICATIONS: May temporarily relieve symptoms of acute or chronic lymphatic congestion, general immune support and lymphatic drainage.** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Mycocombo Allium Cepa, Echinacea (Echinacea Angustifolia), Natrum Sulphuricum, Kali Carbonicum, Mephitis Mephitica, Sanguinaria Canadensis, Blatta Orientalis, Agaricus Muscarius, Antimonium Tartaricum, Arsenicum Iodatum, Carbolicum Acidum, Cinchona Officinalis, Ferrum Metallicum, Phytolacca Decandra, Secale Cornutum, Sulphuricum Acidum, Thuja Occidentalis, Ammonium Carbonicum, Aspergillus Niger ONION ONION ECHINACEA ANGUSTIFOLIA ECHINACEA ANGUSTIFOLIA SODIUM SULFATE SODIUM SULFATE ANHYDROUS POTASSIUM CARBONATE CARBONATE ION MEPHITIS MEPHITIS ANAL GLAND FLUID MEPHITIS MEPHITIS ANAL GLAND FLUID SANGUINARIA CANADENSIS ROOT SANGUINARIA CANADENSIS ROOT BLATTA ORIENTALIS BLATTA ORIENTALIS AMANITA MUSCARIA FRUITING BODY AMANITA MUSCARIA FRUITING BODY ANTIMONY POTASSIUM TARTRATE ANTIMONY CATION (3+) ARSENIC TRIIODIDE ARSENIC CATION (3+) PHENOL PHENOL CINCHONA OFFICINALIS BARK CINCHONA OFFICINALIS BARK IRON IRON PHYTOLACCA AMERICANA ROOT PHYTOLACCA AMERICANA ROOT CLAVICEPS PURPUREA SCLEROTIUM CLAVICEPS PURPUREA SCLEROTIUM SULFURIC ACID SULFURIC ACID THUJA OCCIDENTALIS LEAFY TWIG THUJA OCCIDENTALIS LEAFY TWIG AMMONIUM CARBONATE AMMONIUM CATION ASPERGILLUS NIGER VAR. NIGER ASPERGILLUS NIGER VAR. NIGER ALCOHOL WATER

OTC Limited

HOMEOPATHIC INDICATIONS: For the temporary relief of symptoms of mold toxicity and illness including coughing, wheezing, burning in throat, headache, fatigue, and joint pain.** **These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.

Coumarin Phenolic Coumarinum COUMARIN COUMARIN WATER ALCOHOL

Coumarin Phenolic Coumarinum COUMARIN COUMARIN WATER ALCOHOL 20 %

OTC Limited

INDICATIONS: May temporarily relieve symptoms associated with reactions to coumarin.** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Sciatic Nerve Formula Aesculus hippocastanum, Ammonium muriaticum, Arsenicum album, Belladonna, Capsicum annuum, Causticum, Colchicum autumnale, Colocynthis, Gnaphalium polycephalum, Ignatia amara, Hypericum perforatum, Magnesia phosphorica, Rhus tox, Ruta graveolens HORSE CHESTNUT HORSE CHESTNUT AMMONIUM CHLORIDE AMMONIUM CATION ARSENIC TRIOXIDE ARSENIC CATION (3+) ATROPA BELLADONNA ATROPA BELLADONNA CAPSICUM CAPSICUM CAUSTICUM CAUSTICUM COLCHICUM AUTUMNALE BULB COLCHICUM AUTUMNALE BULB CITRULLUS COLOCYNTHIS FRUIT PULP CITRULLUS COLOCYNTHIS FRUIT PULP PSEUDOGNAPHALIUM OBTUSIFOLIUM WHOLE PSEUDOGNAPHALIUM OBTUSIFOLIUM HYPERICUM PERFORATUM WHOLE HYPERICUM PERFORATUM STRYCHNOS IGNATII SEED STRYCHNOS IGNATII SEED KALMIA LATIFOLIA LEAF KALMIA LATIFOLIA LEAF MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE MAGNESIUM CATION TOXICODENDRON PUBESCENS LEAF TOXICODENDRON PUBESCENS LEAF RUTA GRAVEOLENS FLOWERING TOP RUTA GRAVEOLENS FLOWERING TOP ASCORBIC ACID CITRIC ACID MONOHYDRATE CITRUS AURANTIUM FRUIT OIL ORANGE PEEL CITRUS RETICULATA FRUIT OIL WATER GLYCERIN LACTIC ACID, UNSPECIFIED FORM LONICERA JAPONICA FLOWER POLYEPSILON-LYSINE (4000 MW) CARYA OVATA BARK STEVIOL

OTC Limited

Uses For temporary relief of symptoms: Low back, leg, hip, and joint pain Nerve inflammation Numbness and tingling Weakness in back and legs As per various homeopathic materia medicas. Claims based on traditional homeopathic practice, not accepted medical evidence. These uses have not been evaluated by the FDA, and product has not been clinically tested. Reference image: Sciatic Nerve Formula.jpg

NEUROBALANCE PRO Adrenocorticotrophin, Gaba, Glutamic Acid, norepinephrine, Acetylcholine Chloride, Adrenalinum, L-Dopa, Serotonin, Thyroidinum (Suis) CORTICOTROPIN CORTICOTROPIN .GAMMA.-AMINOBUTYRIC ACID .GAMMA.-AMINOBUTYRIC ACID GLUTAMIC ACID GLUTAMIC ACID NOREPINEPHRINE NOREPINEPHRINE ACETYLCHOLINE CHLORIDE ACETYLCHOLINE EPINEPHRINE EPINEPHRINE LEVODOPA LEVODOPA SEROTONIN SEROTONIN SUS SCROFA THYROID SUS SCROFA THYROID SEMECARPUS ANACARDIUM JUICE SEMECARPUS ANACARDIUM JUICE BARIUM CARBONATE BARIUM CATION OYSTER SHELL CALCIUM CARBONATE, CRUDE OYSTER SHELL CALCIUM CARBONATE, CRUDE DATURA STRAMONIUM DATURA STRAMONIUM WATER ALCOHOL

OTC Limited

INDICATIONS: For the temporary relief of loss of memory, metal weakness, senile dementia, forgetfulness, confusion, anxiety, brain fog, children with slow mental and physical development.

Mycoplasma Homochord Mycoplasma Pneumoniae MYCOPLASMA PNEUMONIAE MYCOPLASMA PNEUMONIAE WATER ALCOHOL

OTC Limited

HOMEOPATHIC INDICATIONS: For temporary relief of symptoms related to Mycoplasma Infection including headache, muscle and joint pain and soreness, and nausea.** **These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.

Cytomegalovirus Homochord Cytomegalovirus Nosode HUMAN HERPESVIRUS 5 HUMAN HERPESVIRUS 5 WATER ALCOHOL

OTC Limited

HOMEOPATHIC INDICATIONS: For the temporary relief of symptoms related to Cytomegalovirus including fever, flu-like symptoms, fatigue, rash and chills.** **These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.

Coumarin Coumarinum COUMARIN COUMARIN WATER ALCOHOL

OTC Limited

INDICATIONS: For temporary relief of abdominal bloating, ear congestion, fatigue, gas, headaches, hay fever, generalized itching, and lower back pain.

Painazol Actaea Spicata, Aesculus Hippocastanum, Arnica Montana, Bellis Perennis, Bryonia (Alba), Calcarea Carbonica, Calcarea Fluorica, Causticum, Cimicifuga Racemosa, Formicum Acidum, Hypericum Perforatum, Ledum Palustre, Lithium Carbonicum, Magnesia Phosphorica, Phosphorus, Phytolacca Decandra, Pulsatilla (Pratensis), Rhododendron Chrysanthum, Rhus Tox, Ruta Graveolens, Salicylicum Acidum, Sepia, Sulphur, Zincum Metallicum SORBITOL SILICON DIOXIDE CROSPOVIDONE COPOVIDONE LACTOSE MONOHYDRATE MAGNESIUM STEARATE MANNITOL MICROCRYSTALLINE CELLULOSE ACTAEA SPICATA ROOT ACTAEA SPICATA ROOT HORSE CHESTNUT HORSE CHESTNUT ARNICA MONTANA ARNICA MONTANA BELLIS PERENNIS BELLIS PERENNIS BRYONIA ALBA ROOT BRYONIA ALBA ROOT OYSTER SHELL CALCIUM CARBONATE, CRUDE OYSTER SHELL CALCIUM CARBONATE, CRUDE CALCIUM FLUORIDE FLUORIDE ION CAUSTICUM CAUSTICUM BLACK COHOSH BLACK COHOSH FORMIC ACID FORMIC ACID HYPERICUM PERFORATUM HYPERICUM PERFORATUM RHODODENDRON TOMENTOSUM LEAFY TWIG LEDUM PALUSTRE TWIG LITHIUM CARBONATE LITHIUM CATION MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE MAGNESIUM CATION PHOSPHORUS PHOSPHORUS PHYTOLACCA AMERICANA ROOT PHYTOLACCA AMERICANA ROOT ANEMONE PRATENSIS ANEMONE PRATENSIS RHODODENDRON AUREUM LEAF RHODODENDRON AUREUM LEAF TOXICODENDRON PUBESCENS LEAF TOXICODENDRON PUBESCENS LEAF RUTA GRAVEOLENS FLOWERING TOP RUTA GRAVEOLENS FLOWERING TOP SALICYLIC ACID SALICYLIC ACID SEPIA OFFICINALIS JUICE SEPIA OFFICINALIS JUICE SULFUR SULFUR ZINC ZINC H

OTC Limited

INDICATIONS FOR USE: For the temporary relief of symptoms such as: • pain • burning • weakness • sensitivity • tingling • numbness Product indications are based solely on Homeopathic Materia Medica and have not been evaluated by the FDA.

BAC Echinacea (Angustifolia), Lomatium Dissectum, Myrrha, Nasturtium Aquaticum, Tabebuia Impetiginosa, Hydrastis Canadensis, Propolis, Glandula Suprarenalis Suis, Lymph Node (Suis), Spleen (Suis), Thymus (Suis), Thyroidinum (Suis), Arsenicum Album, Belladonna, Hypericum Perforatum, Phosphorus, Botulinum, Escherichia Coli, Proteus (Vulgaris), Pseudomonas Aeruginosa, Proteus (Morgani), Salmonella Typhi Nosode, Clostridium Perfringens ECHINACEA ANGUSTIFOLIA ECHINACEA ANGUSTIFOLIA LOMATIUM DISSECTUM ROOT LOMATIUM DISSECTUM ROOT MYRRH MYRRH NASTURTIUM OFFICINALE NASTURTIUM OFFICINALE TABEBUIA IMPETIGINOSA BARK HANDROANTHUS IMPETIGINOSUS BARK GOLDENSEAL GOLDENSEAL PROPOLIS WAX PROPOLIS WAX SUS SCROFA ADRENAL GLAND SUS SCROFA ADRENAL GLAND SUS SCROFA LYMPH SUS SCROFA LYMPH SUS SCROFA SPLEEN SUS SCROFA SPLEEN SUS SCROFA THYMUS SUS SCROFA THYMUS SUS SCROFA THYROID SUS SCROFA THYROID ARSENIC TRIOXIDE ARSENIC CATION (3+) ATROPA BELLADONNA ATROPA BELLADONNA HYPERICUM PERFORATUM HYPERICUM PERFORATUM PHOSPHORUS PHOSPHORUS BOTULINUM TOXIN TYPE A BOTULINUM TOXIN TYPE A ESCHERICHIA COLI ESCHERICHIA COLI PROTEUS VULGARIS PROTEUS VULGARIS PSEUDOMONAS AERUGINOSA PSEUDOMONAS AERUGINOSA PROTEUS MORGANII PROTEUS MORGANII SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR TYPHI SALMONELLA ENTERICA ENTERICA SEROVAR TYPHI CLOSTRIDIUM PERFRINGENS CLOSTRIDIUM PERFRINGENS WATER ALCOHOL

OTC Limited

INDICATIONS: For temporary relief of fever, sore throat and acute irritation of the bladder.

Obsidian 8135 Obsidian PROPRANOLOL HYDROCHLORIDE PROPRANOLOL ALCOHOL WATER

OTC Limited

INDICATIONS Temporarily relieves stubbornness, intolerance, feeling ungrounded or detached, anger, being overly critical or judgmental, or fear.*

Radiation Chondrus crispus, Fucus vesiculosus, Thyroidinum (suis), Cadmium iodatum, Iodium, Strontium carbonicum, X-Ray, CHONDRUS CRISPUS CHONDRUS CRISPUS FUCUS VESICULOSUS FUCUS VESICULOSUS THYROID SUS SCROFA THYROID CADMIUM IODIDE CADMIUM CATION IODINE IODINE STRONTIUM CARBONATE STRONTIUM CATION ALCOHOL, X-RAY EXPOSED (1000 RAD) ALCOHOL, X-RAY EXPOSED (1000 RAD) RADIUM BROMIDE RADIUM CATION WATER ALCOHOL

OTC Limited

INDICATIONS: For temporary relief of symptoms related to mild radiation exposure including weakness, fatigue, exhaustion, fainting, dehydration and diarrhea.

Selenite 8147 Selenite SELENITE ION SELENITE ION ALCOHOL WATER

OTC Limited

INDICATIONS Temporarily relieves mood swings, confusion, feeling of inadequacy, jealousy, or self-doubt.*

Pyrrole Pyrrole PYRROLE PYRROLE WATER ALCOHOL

OTC Limited

HOMEOPATHIC INDICATIONS: For temporary relief of sensitivity to wool, including gas, bloating, and headache.** **These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.

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