Label: YOURGOODSKIN ANTI-ACNE BASE- salicylic acid lotion
- NDC Code(s): 68472-235-30, 68472-235-31
- Packager: BOOTS RETAIL USA INC
- 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 October 31, 2022
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- Active ingredients
- Purpose
- Uses
- Warnings
- When using this product
- Keep out of reach of children.
- GENERAL PRECAUTIONS
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Directions
- Clean the skin thoroughly before applying the product.
- Cover the entire affected area with a thin layer one to three times daily.
- Because excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily if needed or as directed by a doctor.
- If bothersome dryness or peeling occurs, reduce application to once a day or every other day.
- Other information
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Inactive Ingredients
Aqua (Water), Cetearyl Alcohol, Glycerin, Glycereth-7 Trimethyl Ether, Dicapryl Ether, Glyceryl Stearate, PEG-100 Stearate, Neopentyl Glycol Diethylhexanoate, Hydroxyethyl Acrylate Sodium Acryloyldimethyl Taurate Copolymer, Phenoxyethanol, Dicetyl Phosphate, Ceteth-10 Phosphate, Xanthan Gum, Panthenol, Ammonium Glycyrrhizate, Aluminum Starch Octenylsuccinate, Sodium Hydroxide, Parfum (Fragrance), Magnesium Aluminum Silicate, Caprylyl Glycol, Bisabolol, Disodium EDTA, Ethylhexylglycerin, Sorbitan Isostearate, Polysorbate 60, Camellia Sinensis Leaf Extract
- QUESTIONS
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INGREDIENTS AND APPEARANCE
YOURGOODSKIN ANTI-ACNE BASE
salicylic acid lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:68472-235 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 10 mg in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERETH-7 TRIMETHYL ETHER (UNII: XMC7402M60) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) GLYCERIN (UNII: PDC6A3C0OX) CETETH-10 PHOSPHATE (UNII: 4E05O5N49G) HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (100000 MPA.S AT 1.5%) (UNII: 86FQE96TZ4) PHENOXYETHANOL (UNII: HIE492ZZ3T) DIHEXADECYL PHOSPHATE (UNII: 2V6E5WN99N) SODIUM HYDROXIDE (UNII: 55X04QC32I) MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) XANTHAN GUM (UNII: TTV12P4NEE) PANTHENOL (UNII: WV9CM0O67Z) CAPRYLYL GLYCOL (UNII: 00YIU5438U) POLYSORBATE 60 (UNII: CAL22UVI4M) SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4) AMMONIUM GLYCYRRHIZATE (UNII: 3VRD35U26C) PEG-100 STEARATE (UNII: YD01N1999R) NEOPENTYL GLYCOL DIETHYLHEXANOATE (UNII: U68ZV6W62C) LEVOMENOL (UNII: 24WE03BX2T) GREEN TEA LEAF (UNII: W2ZU1RY8B0) DICAPRYLYL ETHER (UNII: 77JZM5516Z) WATER (UNII: 059QF0KO0R) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:68472-235-31 1 in 1 CARTON 12/12/2017 1 NDC:68472-235-30 30 mL in 1 BOTTLE, PLASTIC; 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 12/12/2017 Labeler - BOOTS RETAIL USA INC (143151533)
