Tretinoin cream Tretinoin Cream, a topical retinoid, contains tretinoin 0.025% by weight in a hydrophilic cream vehicle of stearic acid, polyolprepolymer-2, isopropyl myristate, polyoxyl 40 stearate, propylene glycol, stearyl alcohol, xanthan gum, sorbic acid, butylated hydroxytoluene, and purified water. Chemically, tretinoin is all- trans retinoic acid (C 20 H 28 0 2 ; molecular weight 300.44 vitamin A acid) and has the following structural formula: Description: C:\Documents and Settings\MBORTZ\Desktop\image.jpg

Tretinoin cream

Mfr: OTC
FunFoxMeds box

Drug Facts

Composition & Profile

Active Ingredients
Active ingredients (% w/w) Avobenzone 2.5% Octinoxate 3% Octisalate 3% Titanium Dioxide 1.25%
Inactive Ingredients
Inactive ingredients Water Emulsifying Wax Shea butter Stearic Acid Ethylhexyl Palmitate Phenoxyethanol Benzoic Acid Dehydroacetic Acid Sunflower Seed Oil Isopropyl Isostearate Vitamin E Potassium Sorbate Xanthan Gum Sodium Benzoate.
Strengths
0.025 % 20 g 45 g 2.5 % 3 % 1.25 %
Treats Conditions
Indications And Usage Tretinoin Cream Is Indicated For Topical Application In The Treatment Of Acne Vulgaris The Safety And Efficacy Of This Product In The Treatment Of Other Disorders Have Not Been Established Uses Helps Prevent Sunburn If Used As Directed With Other Sun Protection Measures See Directions Decreases The Risk Of Cancer And Early Skin Aging Caused By The Sun

Identifiers & Packaging

Container Type BOX
Packaging

HOW SUPPLIED Tretinoin Cream 0.025% is supplied in 20 g (NDC 0472-0117-20) and 45 g (NDC 0472-0117-45) tubes. Storage Conditions: Store below 30°C (86°F). Avoid freezing. Keep this and all medications out of the reach of children. Manufactured by: G&W NC Laboratories, LLC 1877 Kawai Road Lincolnton, NC 28092 USA Distributed by: Actavis Pharma, Inc. Parsippany, NJ 07054 USA FORM NO. 0117 Rev. 10/14 VC4494; Tretinopak™ - carton: Packaged in the USA by: PureTek Corporation San Fernando, CA 91340 For questions or information call toll-free: 877-921-7873 Rev. 36748 image description

Package Descriptions
  • HOW SUPPLIED Tretinoin Cream 0.025% is supplied in 20 g (NDC 0472-0117-20) and 45 g (NDC 0472-0117-45) tubes. Storage Conditions: Store below 30°C (86°F). Avoid freezing. Keep this and all medications out of the reach of children. Manufactured by: G&W NC Laboratories, LLC 1877 Kawai Road Lincolnton, NC 28092 USA Distributed by: Actavis Pharma, Inc. Parsippany, NJ 07054 USA FORM NO. 0117 Rev. 10/14 VC4494
  • Tretinopak™ - carton: Packaged in the USA by: PureTek Corporation San Fernando, CA 91340 For questions or information call toll-free: 877-921-7873 Rev. 36748 image description

Overview

Tretinoin Cream, a topical retinoid, contains tretinoin 0.025% by weight in a hydrophilic cream vehicle of stearic acid, polyolprepolymer-2, isopropyl myristate, polyoxyl 40 stearate, propylene glycol, stearyl alcohol, xanthan gum, sorbic acid, butylated hydroxytoluene, and purified water. Chemically, tretinoin is all- trans retinoic acid (C 20 H 28 0 2 ; molecular weight 300.44 vitamin A acid) and has the following structural formula: Description: C:\Documents and Settings\MBORTZ\Desktop\image.jpg

Indications & Usage

Tretinoin cream is indicated for topical application in the treatment of acne vulgaris. The safety and efficacy of this product in the treatment of other disorders have not been established. Uses ■ Helps prevent sunburn. ■ If used as directed with other sun protection measures (see Directions), decreases the risk of cancer and early skin aging caused by the sun.

Dosage & Administration

Tretinoin Cream should be applied once a day, in the evening, to the skin where acne lesions appear, using enough to cover the entire affected area lightly. Application may cause a transient feeling of warmth or slight stinging. In cases where it has been necessary to temporarily discontinue therapy or reduce the frequency of application, therapy may be resumed or frequency of application increased when the patients become able to tolerate the treatment. Alterations of dose frequency should be closely monitored by careful observation of the clinical therapeutic response and skin tolerance. Efficacy has not been established for less than once-daily dosing frequencies. During the early weeks of therapy, an apparent increase in number and exacerbation of inflammatory acne lesions may occur. This is due, in part, to the action of the medication on deep, previously unseen lesions and should not be considered a reason to discontinue therapy. Therapeutic results should be noticed after two to three weeks but more than six weeks of therapy may be required before definite beneficial effects are seen. Patients treated with tretinoin cream may use cosmetics, but the areas to be treated should be cleansed thoroughly before the medication is applied (see PRECAUTIONS section). Directions ■ Apply liberally 15 minutes before sun exposure ■ Use a water-resistant sunscreen if swimming or sweating or immediately after towel drying ■ Reaply: ■ 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 the risk, regularly use a sunscreen with a broad spectrum SPF 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. ■ Children under six months of age: Ask a doctor.

Warnings & Precautions
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 Stop use and ask a doctor if ■ rash occurs Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away.
Contraindications

The product should not be used if there is hypersensitivity to any of the ingredients.

Adverse Reactions

The skin of certain sensitive individuals may become excessively red, edematous, blistered, or crusted. If these effects occur, the medication should either be discontinued until the integrity of the skin is restored, or the medication dosing frequency should be adjusted temporarily to a level the patient can tolerate. However, efficacy has not been established for lower dosing frequencies. True contact allergy to topical tretinoin is rarely encountered. Temporary hyper- or hypopigmentation has been reported with repeated application of tretinoin cream. Some individuals have been reported to have heightened susceptibility to sunlight while under treatment with tretinoin cream. Adverse effects of tretinoin cream have been reversible upon discontinuation of therapy (see DOSAGE AND ADMINISTRATION section).

Drug Interactions

Concomitant topical medication, medicated or abrasive soaps and cleansers, soaps and cosmetics that have a strong drying effect, and products with high concentrations of alcohol, astringents, spices or lime should be used with caution because of possible interaction with tretinoin. Particular caution should be exercised in using preparations containing sulfur, resorcinol, or salicylic acid with tretinoin cream. It also is advisable to “rest” a patient’s skin until the effects of such preparations subside before use of tretinoin cream is begun.

Purpose

Purposes Sunscreen (Avobenzone 2.5%) Sunscreen (Octinoxate 3%) Sunscreen (Octisalate 3%) Sunscreen (Titanium Dioxide 1.25%)

Do Not Use

Do not use ■ on damaged or broken skin

When Using

When using this product ■ keep out of eyes ■ Rinse with water to remove

Stop Use & Ask a Doctor

Stop use and ask a doctor if ■ rash occurs

Keep Out of Reach of Children

Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away.

Storage & Handling

Other information ■ Protect this product from excessive heat and direct sun

Questions

Questions? 1.800.611.4270


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