Label: CLEARSKIN PORE PENETRATING BLACK MINERAL MASK- salicylic acid paste
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Contains inactivated NDC Code(s)
NDC Code(s): 10096-0297-1, 10096-0297-2 - 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 January 1, 2019
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- INDICATIONS & USAGE
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WARNINGS
Warnings
For external use only. - DOSAGE & ADMINISTRATION
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INACTIVE INGREDIENT
Inactive ingredients
water/eau, hydrated silica, ethylhexyl palmitate, propylene glycol, bentonite, glycerin, isoceteth-20, PEG-8, magnesium aluminum silicate, camellia sinensis leaf extract, eucalyptus globulus leaf extract, saccharomyces/calcium ferment, saccharomyces/copper ferment, saccharomyces/iron ferment, saccharomyces/ magnesium ferment, saccharomyces/manganese ferment, saccharomyces/potassium ferment, saccharomyces/silicon ferment, saccharomyces/zinc ferment, hamamelis virginiana (witch hazel) extract, polysorbate 20, xanthan gum, sodium methyl cocoyl taurate, butylene glycol, PEG-7 glyceryl cocoate, simethicone, sodium chloride, disodium EDTA, hydroxyethylcellulose, iron oxides, phenoxyethanol, parfum/fragrance. - QUESTIONS
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
CLEARSKIN PORE PENETRATING BLACK MINERAL MASK
salicylic acid pasteProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:10096-0297 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 Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:10096-0297-2 1 in 1 CARTON 03/27/2013 1 NDC:10096-0297-1 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 03/27/2013 Labeler - New Avon LLC (080143520)