Label: PHARMA CLEAR MOISTURIZER- salicylic acid lotion
- NDC Code(s): 67879-103-11
- Packager: PHARMAGEL INTERNATIONAL INC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated January 7, 2024
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENTS
- PURPOSE
- Uses
- WARNINGS
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When using this product:
• avoid contact with the eyes. If product gets into the eyes, rinse thoroughly with water.
• Using other topical acne medications at the same time or immediately following 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.
• Limit use to the face and neck.
- KEEP OUT OF REACH OF CHILDREN
- Directions:
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INACTIVE INGREDIENTS:
WATER (AQUA), DIMETHICONE PEG-8 MEADOWMEADOWFOAMATE, GLYCERETH-26, AMINOMETHYL PROPANOL, CARBOMER, BENZYL ALCOHOL, BETAINE, BISABOLOL, DISODIUM EDTA-COPPER, SODIUM PCA, TRICLOSAN, MELALEUCA ALTERNIFOLIA (TEA TREE) LEAF OIL, PANTHENOL, PEG-40 HYDROGENATED CASTOR OIL, TOCOPHERYL ACETATE, SORBITOL, SERINE, GLYCINE, GLUTAMIC ACID, ALANINE, LYSINE, ARGININE, SODIUM HYALURONATE, THREONINE, PROLINE, RETINYL PALMITATE, ZEA MAYS (CORN) OIL, CHOLECALCIFEROL, ETHYLHEXYLGLYCERIN, HEXYLENE GLYCOL, PHENOXYETHANOL, CAPRYLYL GLYCOL
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
PHARMA CLEAR MOISTURIZER
salicylic acid lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:67879-103 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 1 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) DIMETHICONE PEG-8 LAURATE (UNII: 72MF9C2A18) GLYCERETH-26 (UNII: NNE56F2N14) AMINOMETHYLPROPANOL (UNII: LU49E6626Q) CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E) BENZYL ALCOHOL (UNII: LKG8494WBH) BETAINE (UNII: 3SCV180C9W) LEVOMENOL (UNII: 24WE03BX2T) DISODIUM EDTA-COPPER (UNII: 6V475AX06U) SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2) TRICLOSAN (UNII: 4NM5039Y5X) TEA TREE OIL (UNII: VIF565UC2G) PANTHENOL (UNII: WV9CM0O67Z) POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) SORBITOL (UNII: 506T60A25R) SERINE (UNII: 452VLY9402) GLYCINE (UNII: TE7660XO1C) GLUTAMIC ACID (UNII: 3KX376GY7L) ALANINE (UNII: OF5P57N2ZX) LYSINE (UNII: K3Z4F929H6) ARGININE (UNII: 94ZLA3W45F) HYALURONATE SODIUM (UNII: YSE9PPT4TH) THREONINE (UNII: 2ZD004190S) PROLINE (UNII: 9DLQ4CIU6V) VITAMIN A PALMITATE (UNII: 1D1K0N0VVC) CORN OIL (UNII: 8470G57WFM) CHOLECALCIFEROL (UNII: 1C6V77QF41) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) HEXYLENE GLYCOL (UNII: KEH0A3F75J) PHENOXYETHANOL (UNII: HIE492ZZ3T) CAPRYLYL GLYCOL (UNII: 00YIU5438U) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:67879-103-11 175 mL in 1 TUBE; Type 0: Not a Combination Product 06/15/2016 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M006 06/18/2015 Labeler - PHARMAGEL INTERNATIONAL INC (603215182)