Label: CLEARSKIN BLACKHEAD ELIMINATING DEEP TREATMENT MASK- salicylic acid paste
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Contains inactivated NDC Code(s)
NDC Code(s): 10096-0184-1 - 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 9, 2016
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- 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 product contacts eyes, rinse thoroughly with water. If irritation persists, seek medical attention.
- using other topical acne medications at the same time or immediately after use of this product may increase dryness or irritation of the skin. If this occurs, only one medication should be used unless directed by a doctor.
- DOSAGE & ADMINISTRATION
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INACTIVE INGREDIENT
Inactive ingredients Water/Eau, Hydrated Silica, Ethylhexyl Palmitate,
Propylene Glycol, Glycerin, Isoceteth-20, Cocamidopropyl
Betaine, Chamomilla Recutita (Matricaria)
Flower Extract, Xanthan Gum, PEG-7 Glyceryl
Cocoate, Sodium Chloride, Dimethicone, Menthyl
Lactate, Isododecane, Lysine Carboxymethyl Cysteinate,
Polystyrene/Hydrogenated Polyisopentene
Copolymer, Sodium C8-16 Isoalkylsuccinyl Lactoglobulin
Sulfonate, Disodium EDTA, Phenoxyethanol,
Parfum/Fragrance, Titanium Dioxide/CI 77891,
Blue 1/CI 42090. - QUESTIONS
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
CLEARSKIN BLACKHEAD ELIMINATING DEEP TREATMENT MASK
salicylic acid pasteProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:10096-0184 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Salicylic Acid (UNII: O414PZ4LPZ) (Salicylic Acid - UNII:O414PZ4LPZ) Salicylic Acid 5 mg in 1 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:10096-0184-1 75 mL in 1 TUBE; 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 12/16/2009 Labeler - New Avon LLC (080143520) Establishment Name Address ID/FEI Business Operations Avon Products, Inc. 005149471 manufacture(10096-0184)