Label: ACNE SHAVE MOISTURIZER- salicylic acid cream
-
Contains inactivated NDC Code(s)
NDC Code(s): 65923-112-03 - Packager: United Exchange Corp.
- 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 July 25, 2017
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- WARNINGS
- WHEN USING
- KEEP OUT OF REACH OF CHILDREN
-
INDICATIONS & USAGE
Directions
- cleanse the skin thoroughly before applying this product
- cover the entire affected area with a thin layer one to three times daily
- excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times if needed or as directed by a doctor
- if dryness or peeling occurs, reduce application to once a day or every other day
-
INACTIVE INGREDIENT
Inactive ingredients
Water, Dicaprylyl Carbonate, Pentylene Glycol, Cetearyl Alcohol, Dimethicone, Dicetyl Phosphate, Ceteth-10 Phosphate, Aluminum Starch Octenylsuccinate, Melia Azardirachta Seed Oil, Allantoin, Xanthan Gum, Steareth-20, Hydroxyacetophenone, Methyl Gluceth-20, Tocopheryl Acetate, Aloe Barbadensis Leaf Juice, Caprylyl Glycol, 1,2-Hexanediol, Methyl Lactate, Sodium Hydroxide, Disodium EDTA
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
ACNE SHAVE MOISTURIZER
salicylic acid creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:65923-112 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 0.5 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) DIMETHICONE (UNII: 92RU3N3Y1O) ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294) XANTHAN GUM (UNII: TTV12P4NEE) HYDROXYACETOPHENONE (UNII: G1L3HT4CMH) METHYL GLUCETH-20 (UNII: J3QD0LD11P) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) DICAPRYLYL CARBONATE (UNII: 609A3V1SUA) PENTYLENE GLYCOL (UNII: 50C1307PZG) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) DIHEXADECYL PHOSPHATE (UNII: 2V6E5WN99N) CETETH-10 PHOSPHATE (UNII: 4E05O5N49G) AZADIRACHTA INDICA SEED OIL (UNII: 4DKJ9B3K2T) ALLANTOIN (UNII: 344S277G0Z) STEARETH-20 (UNII: L0Q8IK9E08) CAPRYLYL GLYCOL (UNII: 00YIU5438U) 1,2-HEXANEDIOL (UNII: TR046Y3K1G) METHYL LACTATE, DL- (UNII: H10S91526X) SODIUM HYDROXIDE (UNII: 55X04QC32I) EDETATE DISODIUM (UNII: 7FLD91C86K) ALOE VERA LEAF (UNII: ZY81Z83H0X) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:65923-112-03 98 mL in 1 TUBE; Type 0: Not a Combination Product 07/25/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333D 07/25/2017 Labeler - United Exchange Corp. (840130579)