Drugs Similar to WINCO FOODS SALINE NASAL RELIEF

Straighten the cleaning solution Pour it into the cleaning position for cleaning Usage: This product is designed for gentle cleaning of the face, mouth, nose, eyes,ears, and wounds. It can also be used with a nebulizer to help relieve discomfort in the nose and mouth.

Saline Solution is intended for use in OTC ear,nose,and throat devices intended specifically to administer medicinal substances to treat ear,nose,and throat disorders.These instruments include the powder blower,dropper,ear wick,manual nebulizer pump,and nasal inhaler. If using with an OTC ear,nose,or throat device,the follow the directions provided with the device and only use as directed.

Usage: This product is designed for gentle cleaning of the face, mouth, nose, eyes, ears, and wounds. It can also be used with a nebulizer to help relieve discomfort in the nose and mouth.

Straighten the cleaning solution Pour it into the cleaning position for cleaning

0.9% Sodium Chloride Injection, USP solution is sterile and nonpyrogenic. It is a parenteral solution containing sodium chloride in water for injection intended for intravenous administration. For 0.9% Sodium Chloride Injection, USP, each 100 mL contains 900 mg sodium chloride in water for injection. Electrolytes per 1,000 mL: sodium 154 mEq; chloride 154 mEq. The osmolarity is 308 mOsmol/L (calc.). The pH in the 100 mL and smaller containers is 6.0; for the 250 mL and larger containers, the pH is 5.6. The pH range is 4.5 to 7.0 for all containers. The solution contains no bacteriostat, antimicrobial agent or added buffer and is intended only as a single-dose injection. When smaller doses are required the unused portion should be discarded. The solution is a parenteral fluid and electrolyte replenisher. Sodium Chloride, USP is chemically designated NaCl, a white crystalline powder freely soluble in water. Water for injection, USP is chemically designated H2O. The flexible container is fabricated from a specially formulated non-plasticized, film containing polypropylene and thermoplastic elastomers (freeflex® bag). The amount of water that can permeate from the container into the overwrap is insufficient to affect the solution significantly. Solutions in contact with the flexible container can leach out certain of the container's chemical components in very small amounts within the expiration period. The suitability of the container material has been confirmed by tests in animals according to USP biological tests for plastic containers.

Use For the temporary relief of corneal edema.

Uses for nasal rinsing in adults: Moisturizes and cleanses nasal passages due to pollution, dry air, air conditioning, dust, pollen Nasal drainage Helps dry congestion due to colds and allergies

Runny nose due to allergies, worse in morning*

Uses: See symptoms on front panel. Relieves runny nose due to allergies, worse in morning *

This preparation is designed for parenteral use only after addition of drugs that require dilution or must be dissolved in an aqueous vehicle prior to injection. Bacteriostatic 0.9% Sodium Chloride Injection, USP is a sterile, nonpyrogenic, isotonic solution of sodium chloride in water for injection. Each milliliter (mL) contains sodium chloride 9 mg and 0.9% (9 mg/mL) benzyl alcohol added as a bacteriostatic preservative. May contain hydrochloric acid for pH adjustment. It is supplied in a multiple-dose container from which repeated withdrawals may be made to dilute or dissolve drugs for medication. The pH is 5.0 (4.5 to 7.0). Sodium Chloride, USP is chemically designated NaCl, a white crystalline powder freely soluble in water. The semi-rigid vial is fabricated from a specially formulated polyolefin. It is a copolymer of ethylene and propylene. The safety of the plastic has been confirmed by tests in animals according to USP biological standards for plastic containers. The container requires no vapor barrier to maintain the proper drug concentration.

Bacteriostatic Sodium Chloride Injection, USP, 0.9% is a sterile, nonpyrogenic, isotonic solution. Each mL contains: Sodium chloride 9 mg; benzyl alcohol 0.9%; Water for Injection q.s. Hydrochloric acid and/or sodium hydroxide may have been added for pH adjustment (pH 4.5-7.0). Sodium chloride occurs as colorless cubic crystals or white crystalline powder and has a saline taste. Sodium chloride is freely soluble in water. It is soluble in glycerin and slightly soluble in alcohol. The empirical formula for sodium chloride is NaCl and the molecular weight is 58.44.

This preparation is designed for parenteral use only after addition of drugs that require dilution or must be dissolved in an aqueous vehicle prior to injection. Bacteriostatic 0.9% Sodium Chloride Injection, USP is a sterile, nonpyrogenic, isotonic solution of sodium chloride in water for injection. Each milliliter (mL) contains sodium chloride 9 mg and 0.9% (9 mg/mL) benzyl alcohol added as a bacteriostatic preservative. May contain hydrochloric acid for pH adjustment. It is supplied in a multiple-dose container from which repeated withdrawals may be made to dilute or dissolve drugs for medication. The pH is 5.0 (4.5 to 7.0). Sodium Chloride, USP is chemically designated NaCl, a white crystalline powder freely soluble in water. The semi-rigid vial is fabricated from a specially formulated polyolefin. It is a copolymer of ethylene and propylene. The safety of the plastic has been confirmed by tests in animals according to USP biological standards for plastic containers. The container requires no vapor barrier to maintain the proper drug concentration.

This preparation is designed for parenteral use only after addition of drugs that require dilution or must be dissolved in an aqueous vehicle prior to injection. Bacteriostatic 0.9% Sodium Chloride Injection, USP is a sterile, nonpyrogenic, isotonic solution of sodium chloride in water for injection. Each milliliter (mL) contains sodium chloride 9 mg and 0.9% (9 mg/mL) benzyl alcohol added as a bacteriostatic preservative. May contain hydrochloric acid for pH adjustment. It is supplied in a multiple-dose container from which repeated withdrawals may be made to dilute or dissolve drugs for medication. The pH is 5.0 (4.5 to 7.0). Sodium Chloride, USP is chemically designated NaCl, a white crystalline powder freely soluble in water. The semi-rigid vial is fabricated from a specially formulated polyolefin. It is a copolymer of ethylene and propylene. The safety of the plastic has been confirmed by tests in animals according to USP biological standards for plastic containers. The container requires no vapor barrier to maintain the proper drug concentration.

This preparation is designed for parenteral use only after addition of drugs that require dilution or must be dissolved in an aqueous vehicle prior to injection. Bacteriostatic 0.9% Sodium Chloride Injection, USP is a sterile, nonpyrogenic, isotonic solution of sodium chloride in water for injection. Each milliliter (mL) contains sodium chloride 9 mg and 0.9% (9 mg/mL) benzyl alcohol added as a bacteriostatic preservative. May contain hydrochloric acid for pH adjustment. It is supplied in a multiple-dose container from which repeated withdrawals may be made to dilute or dissolve drugs for medication. The pH is 5.0 (4.5 to 7.0). Sodium Chloride, USP is chemically designated NaCl, a white crystalline powder freely soluble in water. The semi-rigid vial is fabricated from a specially formulated polyolefin. It is a copolymer of ethylene and propylene. The safety of the plastic has been confirmed by tests in animals according to USP biological standards for plastic containers. The container requires no vapor barrier to maintain the proper drug concentration.

Uses : For dry nasal membranes

Uses : For dry nasal membranes

Uses : For dry nasal membranes

Use Temporarily relieves symptons associated with sinusitis, cold, flu, allergies Including: Post nasal drip, sneezing, runny nose, nasal stuffiness Removes inhaled irritants, dust, pollen Helps reduce swelling of nasal membranes Moistens dry nasal passages Promotes nasal and sinus clearage

Uses Nasal congestion Removes inhaled irritants (dust, dirt, pollen) Moisturizes dry nasal passages

Uses Nasal congestion Removes inhaled irritants (dust, dirt, pollen) Moisturizes dry nasal passages

Straighten the cleaning solution Pour it into the cleaning position for cleaning Usage: This product is designed for gentle cleaning of the face, mouth, nose, eyes,ears, and wounds. It can also be used with a nebulizer to help relieve discomfort in the nose and mouth.

Saline Solution is intended for use in OTC ear,nose,and throat devices intended specifically to administer medicinal substances to treat ear,nose,and throat disorders.These instruments include the powder blower,dropper,ear wick,manual nebulizer pump,and nasal inhaler. If using with an OTC ear,nose,or throat device,the follow the directions provided with the device and only use as directed.

Usage: This product is designed for gentle cleaning of the face, mouth, nose, eyes, ears, and wounds. It can also be used with a nebulizer to help relieve discomfort in the nose and mouth.

Straighten the cleaning solution Pour it into the cleaning position for cleaning

Sodium Chloride Injection, USP is a sterile, nonpyrogenic solution for fluid and electrolyte replenishment in single dose containers for intravenous administration. It contains no antimicrobial agents. The pH ranges from 4.5 to 7.0. Composition, osmolarity, and ionic concentration are shown below: 0.9% Sodium Chloride Injection, USP contains 9 g/L Sodium Chloride, USP (NaCl) with an osmolarity of 308 mOsmol/L (calc). It contains 154 mEq/L sodium and 154 mEq/L chloride. The FLEBOFLEX and FLEBOFLEX LUER plastic containers are fabricated from latex-free polyolefins or polypropylene plastic materials. The solution contact materials do not contain PVC, DEHP, or other plasticizers. The amount of water that can permeate from inside the container into the overwrap is insufficient to affect the solution significantly. The suitability of the container materials has been established through biological evaluations, which have shown the containers pass Class VI U.S. Pharmacopeia (USP) testing for plastic containers. These tests confirm the biological safety of the container systems.

Sodium Chloride Injection, USP solutions are sterile and nonpyrogenic. They are parenteral solutions containing various concentrations of sodium chloride in water for injection intended for intravenous administration. For 0.45% Sodium Chloride Injection, USP, each 100 mL contains 450 mg sodium chloride in water for injection. Electrolytes per 1000 mL: sodium 77 mEq; chloride 77 mEq. The osmolarity is 154 mOsmol/L (calc.). For 0.9% Sodium Chloride Injection, USP, each 100 mL contains 900 mg sodium chloride in water for injection. Electrolytes per 1000 mL: sodium 154 mEq; chloride 154 mEq. The osmolarity is 308 mOsmol/L (calc.). The pH for both concentrations in the 100 mL and smaller containers is 6.0; for the 250 mL and larger containers, the pH is 5.6. The pH range is 4.5 to 7.0 for all containers. The solutions contain no bacteriostat, antimicrobial agent or added buffer and each is intended only as a single-dose injection. When smaller doses are required the unused portion should be discarded. The solutions are parenteral fluid and electrolyte replenishers. Sodium Chloride, USP is chemically designated NaCl, a white crystalline powder freely soluble in water. Water for Injection, USP is chemically designated H2O. The flexible plastic container is fabricated from a specially formulated polyvinylchloride. Water can permeate from inside the container into the overwrap but not in amounts sufficient to affect the solution significantly. Solutions in contact with the plastic container may leach out certain chemical components from the plastic in very small amounts; however, biological testing was supportive of the safety of the plastic container materials. Exposure to temperatures above 25°C (77°F) during transport and storage will lead to minor losses in moisture content. Higher temperatures lead to greater losses. It is unlikely that these minor losses will lead to clinically significant changes within the expiration period.

This preparation is designed solely for parenteral use only after addition of drugs that require dilution or must be dissolved in an aqueous vehicle prior to injection. 0.9% Sodium Chloride Injection, USP is a sterile, nonpyrogenic, isotonic solution of sodium chloride and water for injection. Each mL contains sodium chloride 9 mg. It contains no bacteriostat, antimicrobial agent or added buffer and is supplied only in single-dose containers to dilute or dissolve drugs for injection. 0.308 mOsmol/mL (calc.). 0.9% Sodium Chloride Injection, USP contains no preservatives. The solution may contain hydrochloric acid and/or sodium hydroxide for pH adjustment. pH 5.3 (4.5 to 7.0). Sodium Chloride, USP is chemically designated NaCl, a white crystalline compound freely soluble in water. The glass container is a Type I borosilicate glass and meets the requirements of the powdered glass test according to the USP standards. The semi-rigid vial is fabricated from a specially formulated polyolefin. It is a copolymer of ethylene and propylene. The safety of the plastic has been confirmed by tests in animals according to USP biological standards for plastic containers. The container requires no vapor barrier to maintain the proper drug concentration.

Sodium Chloride Injection, USP solutions are sterile and nonpyrogenic. They are parenteral solutions containing various concentrations of sodium chloride in water for injection intended for intravenous administration. For 0.45% Sodium Chloride Injection, USP, each 100 mL contains 450 mg sodium chloride in water for injection. Electrolytes per 1000 mL: sodium 77 mEq; chloride 77 mEq. The osmolarity is 154 mOsmol/L (calc.). For 0.9% Sodium Chloride Injection, USP, each 100 mL contains 900 mg sodium chloride in water for injection. Electrolytes per 1000 mL: sodium 154 mEq; chloride 154 mEq. The osmolarity is 308 mOsmol/L (calc.). The pH for both concentrations in the 100 mL and smaller containers is 6.0; for the 250 mL and larger containers, the pH is 5.6. The pH range is 4.5 to 7.0 for all containers. The solutions contain no bacteriostat, antimicrobial agent or added buffer and each is intended only as a single-dose injection. When smaller doses are required the unused portion should be discarded. The solutions are parenteral fluid and electrolyte replenishers. Sodium Chloride, USP is chemically designated NaCl, a white crystalline powder freely soluble in water. Water for Injection, USP is chemically designated H2O. The flexible plastic container is fabricated from a specially formulated polyvinylchloride. Water can permeate from inside the container into the overwrap but not in amounts sufficient to affect the solution significantly. Solutions in contact with the plastic container may leach out certain chemical components from the plastic in very small amounts; however, biological testing was supportive of the safety of the plastic container materials. Exposure to temperatures above 25°C (77°F) during transport and storage will lead to minor losses in moisture content. Higher temperatures lead to greater losses. It is unlikely that these minor losses will lead to clinically significant changes within the expiration period.

Sodium Chloride Injection, USP solutions are sterile and nonpyrogenic. They are parenteral solutions containing various concentrations of sodium chloride in water for injection intended for intravenous administration. For 0.45% Sodium Chloride Injection, USP, each 100 mL contains 450 mg sodium chloride in water for injection. Electrolytes per 1000 mL: sodium 77 mEq; chloride 77 mEq. The osmolarity is 154 mOsmol/L (calc.). For 0.9% Sodium Chloride Injection, USP, each 100 mL contains 900 mg sodium chloride in water for injection. Electrolytes per 1000 mL: sodium 154 mEq; chloride 154 mEq. The osmolarity is 308 mOsmol/L (calc.). The pH for both concentrations in the 100 mL and smaller containers is 6.0; for the 250 mL and larger containers, the pH is 5.6. The pH range is 4.5 to 7.0 for all containers. The solutions contain no bacteriostat, antimicrobial agent or added buffer and each is intended only as a single-dose injection. When smaller doses are required the unused portion should be discarded. The solutions are parenteral fluid and electrolyte replenishers. Sodium Chloride, USP is chemically designated NaCl, a white crystalline powder freely soluble in water. Water for Injection, USP is chemically designated H2O. The flexible plastic container is fabricated from a specially formulated polyvinylchloride. Water can permeate from inside the container into the overwrap but not in amounts sufficient to affect the solution significantly. Solutions in contact with the plastic container may leach out certain chemical components from the plastic in very small amounts; however, biological testing was supportive of the safety of the plastic container materials. Exposure to temperatures above 25°C (77°F) during transport and storage will lead to minor losses in moisture content. Higher temperatures lead to greater losses. It is unlikely that these minor losses will lead to clinically significant changes within the expiration period.

0.9% Sodium Chloride Injection, USP solution is sterile and nonpyrogenic. It is a parenteral solution containing sodium chloride in water for injection intended for intravenous administration. For 0.9% Sodium Chloride Injection, USP, each 100 mL contains 900 mg sodium chloride in water for injection. Electrolytes per 1,000 mL: sodium 154 mEq; chloride 154 mEq. The osmolarity is 308 mOsmol/L (calc.). The pH in the 100 mL and smaller containers is 6.0; for the 250 mL and larger containers, the pH is 5.6. The pH range is 4.5 to 7.0 for all containers. The solution contains no bacteriostat, antimicrobial agent or added buffer and is intended only as a single-dose injection. When smaller doses are required the unused portion should be discarded. The solution is a parenteral fluid and electrolyte replenisher. Sodium Chloride, USP is chemically designated NaCl, a white crystalline powder freely soluble in water. Water for injection, USP is chemically designated H2O. The flexible container is fabricated from a specially formulated non-plasticized, film containing polypropylene and thermoplastic elastomers (freeflex® bag). The amount of water that can permeate from the container into the overwrap is insufficient to affect the solution significantly. Solutions in contact with the flexible container can leach out certain of the container's chemical components in very small amounts within the expiration period. The suitability of the container material has been confirmed by tests in animals according to USP biological tests for plastic containers.

USES: COLDS, HEADACHES, EXHAUSTION, NERVOUSNESS, SKIN AND DIGESTIVE ISSUES** **C, K, CK & X ARE HOMEOPATHIC DILUTIONS.

INDICATIONS: For weight management and inflammation support. This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.

3% Sodium Chloride Injection, USP is a sterile, nonpyrogenic, hypertonic solution for fluid and electrolyte replenishment in single dose containers for intravenous administration. The pH may have been adjusted with hydrochloric acid. It contains no antimicrobial agents. Composition, ionic concentration, osmolarity, and pH are shown in Table 1 . Table 1. *Normal physiological osmolarity range is approximately 280 to 310 mOsmol/L. Size (mL) Composition (g/L) Ionic Concentration (mEq/L) *Osmolarity (mOsmol/L) (calc) pH Sodium Chloride, USP (NaCl) Sodium Chloride 3% Sodium Chloride Injection, USP 500 30 513 513 1,027 5.0 (4.5 to 7.0) The flexible container is fabricated from a specially formulated non-plasticized, film containing polypropylene and thermoplastic elastomers (free flex ® bag). The amount of water that can permeate from the container into the overwrap is insufficient to affect the solution significantly. Solutions in contact with the flexible container can leach out certain of the container's chemical components in very small amounts within the expiration period. The suitability of the container material has been confirmed by tests in animals according to USP biological tests for plastic containers.

Uses Temporarily relieves the symptoms of the common cold including: nasal or chest congestion, runny nose, sore throat, sneezing, cough.

Uses* ■ Helps temporarily relieve symptoms of common cold in children at night, including: ■ cough ■ runny nose ■ post nasal drip ■ sneezing ■ sore throat ■ nasal or chest congestion ■ occasional sleeplessness

Uses ■ Helps temporarily relieve symptoms of common cold in children at night, including: ■ cough ■ runny nose ■ post nasal drip ■ sneezing ■ sore throat ■ nasal or chest congestion ■ occasional sleeplessness

Uses Temporarily relieves the symptoms of the common cold in children especially at night including accumulation of mucus in chest, throat and nose, cough with mucus, runny nose, sneezing, nasal congestion and occasional sleeplessness.

Uses* ■ Helps temporarily relieve symptoms of common cold in children, including: ■ runny nose ■ sore throat ■ sneezing ■ cough ■ post nasal drip ■ nasal or chest congestion

Uses ■Temporarily relieves symptoms of common cold in children, including: ■ accumulation of mucus in chest, throat or nose ■ cough with expectoration of thick, discolored mucus ■ runny nose ■ sneezing ■ nasal or chest congestion

Uses † for temporary relief of: physical fatigue mental and emotional fatigue nervous exhaustion sluggish mind poor concentration weariness confusion apathy irritability indifference body aches lack of focus eyes sensitive to light digestive symptoms caused by stress light-headed upon standing up † Claims based on traditional Homeopathic practice, not accepted medical evidence, not FDA evaluated.

Uses For tocipal irrigation of eyes, burns and wounds

Product name Ginsamin Energy Active ingredients Ginkgo leaf extract, Korean ginseng root extract, Creatine, Taurine, Vitamin C Inactive ingredients vitamin A, vitamin B1, riboflavin, vitamin B6, vitamin B12, L-cystine, blueberry, purified water, selenium yeast, honey, citric acid, fructose Effect • improve the body's ability to handle fatigue and stress • support mental alertnss and an energetic feeling all day long • provide nutritional support for increased brain energy • strengthen immunity against colds and flus and other infections • improve learning, memory and mental function • improve physical performance capacity Warning If you have an allergic reaction after taking it, consult your doctor Caution • Store at room temperature. • Keep out of reach of children. • Avoid exposing the product direct to sunlight, high temperatures and humidity. • Manufacturer Manufacturer Biogrand, lnc / B-905, Woolim Lion’s Valley, 371-28 Gasan-dong, Geumcheon-gu, Seoul 153-786, Korea

Use Temporarily relieves minor pain Warnings For external use only Do not use: more than 1 patch on your body at a time on cut, irritated or swollen skin on puncture wounds for more than one week without consulting a doctor at the same time as other topical analgesics When using this product: • use only as directed. • read and follow all directions and warnings on this label • rare cases of serious burns have been reported with products of this type. • do not apply to wounds or damaged, broken • eyes and mucous membranes • do not bandage tightly or apply local heat (such as • the same time as other topical analgesics • keeps product away from children and pets. used patches still contain the drug product that can produce serious adverse effects if a child or pet chews or ingests this patch. • a transient burning sensation may occur upon application but generally disappears in several days • if a severe burning sensation occurs, discontinue use immediately. • discontinue use at least 1 hour before a bath or shower. • do not use immediately after a bath or shower. Stop use and ask doctor if: • condition worsen • redness is present • irritation develops • symptoms persist for more than 7 days or clear up and occur again within a few days • you experience signs of skin injury, such as pain, swelling, or blistering where this product is applied if pregnant or breast feeding, ask a health professional before use. keep out of reach of children and pets If swallowed, get medical help or contact a Poison Control Center right away. Directions: Adult and children over 12years: Clean and dry affected area remove backing from patch by firmly grasping both ends and gently pulling until back separates in middle Carefully remove smaller portion of backing from the patch and apply exposed portion of patch to affected area use 1 patch for up to 12 hours children 12 years or younger: ask a doctor Inactive ingredients: Alpha Tocopherol, Aluminum Sulphate, Borax, Carbomer, Colloidal Silicon Dioxide, DMDM Hydantoin, Glycerin, Kaolin, Polyacrylic Acid, Polyvinyl Alcohol, Polyvinylpyrrolidone , Propylene Glycol, Purified Water, Sodium Carboxymethyl Cellulose, Sodium Ethylenediaminetetraacetic Acid, Sodium Polyacrylate, Sorbitol, Sorbitol Monooleate , Tartaric Acid & Titanium Dioxide Other Information: Store at room temperature 20·25'C (68-77'F) Questions? call toll-free 1-844-912-4012

Indications For relief of yeast infections.

Stop use and ask a doctor if rash occurs. Warnings For external use only Do not use on damaged or broken skin When using this product keep out of eyes. Rinse with water to remove Directions Apply foundation to a clean face for Broad Spectrum protection. Reapply as needed. This is not a primary sunscreen. For further protection by a primary sunscreen follow directions below. Apply primary sunscreen liberally 15 minutes before sun exposure Reapply: At least 2 hours Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF 15 or higher and other sun protection measures including: Limit time in the sun, especially from 10 a.m. - 2p.m. Wear long-sleeve shirts, pants, hats, and sunglasses Children under 6 months ask doctor. Inactive Ingredients: Water/Aqua, Cyclomethicone, Butylene Glycol, Isononyl Isononoate, Behenyl Dimethicone, Cetyl PEG/PPG-10/1 Dimethicone, Phenyl Trimethicone, C12-15 Alkyl Benzoate, Disteardimonium Hectorite, Glcyeryl Ethylhexanoate/Stearate/Adipate, Phenoxyethanol, Sucrose Acetyl Isobutyrate, Tocopheryl Acetate, Sodium Chloride, Lauryl PEG-8 Dimethicone, Alumina, Sodium Dehydroacetate, Methicone, Triethoxycaprylylsilane, Caprylic/Capric Triglyceride, Trisodium Ethylenediamine Dissucinate, Dimethicone, Tropolone, Tripeptide-3, Hexapeptide-3, (May contain (+/-) CI 77891 (Titanium Dioxide), CI 77491 (iron oxides), CI 77492 (Iron Oxides), CI 77499 (Iron Oxides).

Discontinue if signs of irritation appear.

Stop use and ask a doctor if rash occurs warnings For external use only Do not use on damaged or broken skin When using this product keep out of eyes. Rinse with water to remove. Directions apply daily under the eye and along the brow line apply liberally 15 minutes before sun exposure children under 6 months of age: Ask a doctor reapply at least every 2 hours use a water resistant sunscreen of swimming or sweating Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including: Limit time in the sun, especially from 10 a.m. – 2 p.m. Wear long-sleeve shirts, pants, hats, and sunglasses Inactive Ingredients: Water (Aqua), Cetearyl Alcohol, Soybean Glycerides, Butyrospermum Parkii (Shea Butter) Unsaponifiables, Polyethylene, Myristyl Myristate, Ethoxydiglycol, Butylene Glycol, Synthetic Beeswax, Glyceryl Caprylate, Glycoproteins, Panax Ginseng Root Extract, Equisetum Arvense (Horsetail) Extract, Hesperetin Laurate, Saccharomyces/Xylinum/Black Tea Ferment, Tocopherol, Hydrolyzed Malt Extract, Lecithin, Olea Europaea (Olive) Oil Unsaponifiables, Ursolic Acid, Erythrityl Triethylhexanoate, Plankton Extract, Ilomastat, Carnosine, Echium Plantagineum Seed Oil, Carbomer, Caprylyl/Capryl Glucoside, Serine, Silybum Marianum Fruit Extract, Acacia Senegal Gum, Ascorbyl Tetraisopalmitate, Triticum Vulgare (Wheat) Germ Oil Unsaponifiables, Hydroxyethylcellulose, Lauroyl Lysine, Melissa Officinalis Leaf Extract, PEG-8, Pollen Extract, Hydrogenated Lecithin, Glycerin, Trehalose, Glycine Soja (Soybean) Oil Unsaponifiables, Polyquaternium-51, Sodium Hyaluronate, Camellia Sinensis Leaf Extract, Sodium Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, PEG-6 Isostearate, Propylene Glycol, Cyclopentasiloxane, Caprylic/Capric Triglyceride, Urea, Sodium PCA, Isodecyl Salicylate, Tocopheryl Linoleate/Oleate, Algin, Disodium EDTA, Isopropylbenzyl Salicylate, Steareth-2, Phospholipids, DNA, Polyisobutene, Ceteth-20, Xanthan Gum, Triacetin, Mica, Cyclomethicone, Polymethyl Methacrylate, Steareth-21, Cyclohexasiloxane, Sucrose, Stearic Acid, Alcohol, Aluminum Hydroxide, Fragrance (Parfum), Benzyl Alcohol, Linalool, Hydroxycitronellal, Alpha-Isomethyl Ionone, Amyl Cinnamal, Hexyl Cinnamal, Evernia Furfuracea (Treemoss) Extract, Geraniol, Benzyl Benzoate, Butylphenyl Methylpropional, Phenoxyethanol, Benzoic Acid, Methylparaben, Potassium Sorbate, Chlorphenesin, Ethylparaben, Butylparaben, Propylparaben, Isobutylparaben, Titanium Dioxide (CI 77891)

Stop use and ask a dcotor if rash occurs. Warnings For external use only Do not use on damaged or broken skin When using this product keep out of eyes. Rinse with water to remove. Directions Apply foundation liberally to clean face for Broad Spectrum protection. Reapply as needed. This is not a primary Sunscreen. For further protection by a primary Sunscreen follow directions below. Apply primary Sunscreen liberally 15 minutes before sun exposure Reapply at least every 2 hours. Sun Protection measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a broad spectrum SPF 15 or higher and other sun protection measures including: Limit time in the sun, especially 10 a.m. - 2 p.m. Wear long-sleeve shirts, pants, hats, and sunglasses Children under 6 months ask doctor Inactive Ingredients: Water/Aqua, Cyclomethicone, Butylene Glycol, Isononyl Isononoate, Behenyl Dimethicone, Cetyl PEG/PPG-10/1 Dimethicone, Phenyl Trimethicone, C12-15 Alkyl Benzoate, Disteardimonium Hectorite, Glcyeryl Ethylhexanoate/Stearate/Adipate, Phenoxyethanol, Sucrose Acetyl Isobutyrate, Tocopheryl Acetate, Sodium Chloride, Lauryl PEG-8 Dimethicone, Alumina, Sodium Dehydroacetate, Methicone, Triethoxycaprylylsilane, Caprylic/Capric Triglyceride, Trisodium Ethylenediamine Dissucinate, Dimethicone, Tropolone, Tripeptide-3, Hexapeptide-4, (May contain (+/-) CI 77891 (Titanium Dioxide), CI 77491 (iron oxides), CI 77492 (Iron Oxides), CI 77499 (Iron Oxides).

Summary not available yet.

Stop use and ask a doctor if rash or irritation develops and lasts.

indications Stop use and ask a doctor if rash occurs. warnings Warnings For external use only. Do not use on damaged or broken skin. When using this product keep out of eyes. Rinse with water to remove. Directions apply daily after cleansing and toning smooth over body apply liberally 15 minutes before sun exposure children under 6 months of age: Ask a doctor reapply at least every 2 hours use a water resistant sunscreen if swimming or sweating Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including: Limit time in the sun, especially from 10 a.m. – 2 p.m. Wear long-sleeve shirts, pants, hats, and sunglasses Inactive ingredients Water (Aqua), Caprylyl Methicone, Undecrylene Dimethicone, Polyester-8, Polyglyceryl-3 Methylglucose Distearate, Butylene Glycol, Pentylene Glycol, Steareth-21, Glycoproteins, Panax Ginseng Root Extract, Equisetum Arvense (Horsetail) Extract, Sodium Hyaluronate, Octyldodecyl Olivate, Allantoin, Porphyra Umbilicalis Extract, Tocopheryl Acetate, Benzylidene Dimethoxydimethylindanone, Sea Water (Maris Aqua), Diethylhexyl Syringyldenemalonate, Polyacrylamide, Pelvetia Canaliculata Extract, Lecithin, Caprylic/Capric Triglyceride, Palmaria Palmata Extract, Ethylhexylglycerin, Algae Extract, Steareth-2, Disodium EDTA, Hydroxypropyl Starch Phosphate, Alcohol, C13-14 Isoparaffin, Sodium Lactate, Stearyl Alcohol, Dipropylene Glycol, Laureth-7, Fragrance (Parfum), Benzyl Alcohol, Phenoxyethanol, Chlorphenesin, Methylparaben, Propylparaben

Indications For flu symptoms and infections

Indications For treatment of circulatory symptoms and blood-related conditions.

Discontinue use if signs of irritation occur.

INDICATIONS & USAGE SECTION Other information store at 15 o -30 o C (59 o -86 o F) Label

Stop use and ask a doctor if: rash occurs. Warnings For external use only. Do not use on damaged or broken skin. When using this product keep out of eyes. Rinse with water to remove. Directions ■ Apply liberally and evenly 15 minutes before sun exposure. Sun Protection Measures: Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including: ■ Limit time in the sun, especially from 10a.m.- 2 p.m. ■ Wear long-sleeved shirts, pants, hats, and sunglasses. ■ Reapply at least every 2 hours. ■ Use a water resistant sunscreen if swimming or sweating. ■ Children under 6 months of age: ask doctor. Water (Aqua/Eau), Titanium Dioxide, C12-15 Alkyl Benzoate, Steareth-21, Glycerin, Glyceryl Stearate, Propanediol, Caprylic/Capric Triglyceride, Polymethylsilsesquioxane, Dimethicone, Lauryl Phenylpropyl Methicone, Caprylyl Methicone, Cetearyl Alcohol, PPG-12/SMDI Copolymer, Iron Oxides, Triheptanoin, Mica, Fragrance, PEG-100 Stearate, Phenoxyethanol, Glycine Soja (Soybean) Seed Extract, Limonene, Cyclopentasiloxane, Caprylyl Glycol, Diethylhexyl Syringylidenemalonate, Aminomethyl Propanol, Vaccinium Myrtillus Fruit Extract, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Acrylates/Dimethicone Copolymer, Ethylhexylglycerin, Trisodium Ethylenediamine Disuccinate, Ferulic Acid, Laminaria Ochroleuca Extract, Tocopheryl Acetate, Saccharum Officinarum (Sugar Cane) Extract, Hexylene Glycol, Triethoxycaprylylsilane, Tin Oxide, Flavor, Sodium Citrate, Citrus Aurantium Dulcis (Orange) Fruit Extract, Citrus Medica Limonum (Lemon) Fruit Extract, Citrus Aurantium Dulcis (Orange) Flower Extract, Rosa Canina Seed Extract, Hydrolyzed Viola Tricolor Extract, Citrus Grandis (Grapefruit) Fruit Extract, Linalool, Acer Saccharum (Sugar Maple) Extract, Sodium Hyaluronate, Ceramide 2, Citral, Butylene Glycol, Benzyl Benzoate, Palmitoyl Tripeptide-5, Benzyl Alcohol, 3-O-Ethyl Ascorbic Acid, Tetrahexyldecyl Ascorbate, Camellia Sinensis Leaf Extract.

Indications For liver detoxification, eczema, dermatitis and minor skin irritation.

Summary not available yet.

Summary not available yet.

USES helps loosen phlegm (mucus) and thin bronchial secretions to make coughs more productive temporarily relieves cough due to minor throat and bronchial irritation as may occur with a cold