Label: SALICYLIC ACID cream
- NDC Code(s): 80861-117-01
- Packager: Acne Free, LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated June 19, 2024
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- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Use
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Warnings
For external use only
When using this product
When using this product skin irritation and dryness is more likely to occur if you use another topical acne medication at the same time. If irritation occurs, only use one topical acne medication at a time.
- Directions
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Inactive Ingredients
water, cocamidopropyl betaine, sodium cocoyl isethionate, glycerin, coco-glucoside, hydrogenated castor oil, acrylates/C10-30 alkyl acrylate crosspolymer, sodium hydroxide, sodium benzoate, avena sativa (oat) kernel oil, guar hydroypropyltrimonium chloride, hydrogenated jojoba oil, zingiber of cinale (ginger) root juice, charcoal powder, iron oxides (CI 77499)
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- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
SALICYLIC ACID
salicylic acid creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:80861-117 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 0.02 g in 1 g Inactive Ingredients Ingredient Name Strength COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:80861-117-01 1 g in 1 TUBE; Type 0: Not a Combination Product 02/05/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M006 02/05/2024 Labeler - Acne Free, LLC (122237140) Establishment Name Address ID/FEI Business Operations Paklab 177711082 manufacture(80861-117)