Label: YOURGOODSKIN CALMING CLEANSER- salicylic acid cream
- NDC Code(s): 68472-236-13, 68472-236-14
- 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 March 27, 2022
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- Official Label (Printer Friendly)
- Active ingredients
- Purpose
- Uses
- Warnings
- When using this product
- Keep out of reach of children.
- Avoid contact with eyes.
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Directions
- Wet your face with warm water before dispensing the cleanser into your hands.
- Massage into your face in circular motions, working from the centre of the face outwards, avoiding contact with the delicate eye area.
- Rinse away with warm water. Try not to have the water too hot as this can dry your skin.
- Use daily and follow with your Balancing Skin Concentrate.
- Other information
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Inactive Ingredients
Aqua (Water), Cetyl Alcohol, Glycereth-7 Trimethyl Ether, Cera Microcristallina (Microcrystalline Wax), Ceteareth-20, Polysorbate 60, Hydroxyethyl Acrylate/Sodium Acryloldimethyl Taurate Copolymer, Potassium Cetyl Phosphate, Phenoxyethanol, Parfum (Fragrance), Sodium Hydroxide, Ammonium Glycyrrhizate, Panthenol, Xanthan Gum, Capryly Glycol, Ethylhexylglycerin, Sorbitan Isostearate, Bisabolol, Camellia Sinensis Leaf Extract.
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
YOURGOODSKIN CALMING CLEANSER
salicylic acid creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:68472-236 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 POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT) MICROCRYSTALLINE WAX (UNII: XOF597Q3KY) HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (100000 MPA.S AT 1.5%) (UNII: 86FQE96TZ4) PHENOXYETHANOL (UNII: HIE492ZZ3T) SODIUM HYDROXIDE (UNII: 55X04QC32I) XANTHAN GUM (UNII: TTV12P4NEE) PANTHENOL (UNII: WV9CM0O67Z) CAPRYLYL GLYCOL (UNII: 00YIU5438U) POLYSORBATE 60 (UNII: CAL22UVI4M) SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4) AMMONIUM GLYCYRRHIZATE (UNII: 3VRD35U26C) GREEN TEA LEAF (UNII: W2ZU1RY8B0) POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY) WATER (UNII: 059QF0KO0R) CETYL ALCOHOL (UNII: 936JST6JCN) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) GLYCERETH-7 TRIMETHYL ETHER (UNII: XMC7402M60) .ALPHA.-BISABOLOL, (+/-)- (UNII: 36HQN158VC) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:68472-236-14 1 in 1 CARTON 05/16/2017 1 NDC:68472-236-13 125 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 05/16/2017 Labeler - BOOTS RETAIL USA INC (143151533)