Label: CLEARSKIN BLACKHEAD ELIMINATING DAILY ASTRINGENT- salicylic acid liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 10096-0320-1 - Packager: New Avon LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated February 19, 2016
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- INDICATIONS & USAGE
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WARNINGS
Warnings
For external use only.
When using this product
- avoid contact with eyes. If contact occurs, rinse thoroughly with water.
- skin irritation and dryness is more likely to occur if you use another topical acne medication at the same time. If irritation occurs, use only one topical acne medication at a time unless directed by a health care practitioner.
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DOSAGE & ADMINISTRATION
Directions
- Cleanse the skin thoroughly before applying the product.
- Moisten cotton ball and cover the entire affected area with a thin layer one to three times daily.
- Gently work moistened cotton ball over face and neck. Do not rinse.
- Because excessive drying of the skin may occur, start with one application daily, then gradually increase to two to three times daily if needed or as directed by a health care practitioner.
- If bothersome dryness or peeling occurs, reduce application to once a day or every other day.
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INACTIVE INGREDIENT
Inactive ingredients SD alcohol 40-B, water/eau, propylene glycol, PEG-6, potassium hydroxide, benzophenone-1, parfum/fragrance, BHT, disodium EDTA, lysine carboxymethyl cysteinate, isododecane, aloe barbadensis leaf juice, sodium C8-16 isoalkylsuccinyl lactoglobulin sulfonate, polystyrene/
hydrogenated polyisopentene copolymer, chamomilla recutita (matricaria) flower extract, blue 1/CI 42090, red 33/CI 17200. - QUESTIONS
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
CLEARSKIN BLACKHEAD ELIMINATING DAILY ASTRINGENT
salicylic acid liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:10096-0320 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Salicylic Acid (UNII: O414PZ4LPZ) (Salicylic Acid - UNII:O414PZ4LPZ) Salicylic Acid 20 mg in 1 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:10096-0320-1 250 mL in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333D 03/17/2014 Labeler - New Avon LLC (080143520) Establishment Name Address ID/FEI Business Operations Avon Products, Inc. 005149471 manufacture(10096-0320)