Label: YOURGOODSKIN BLACKHEAD CLEARING SCRUB- salicylic acid cream
- NDC Code(s): 68472-238-13, 68472-238-14
- 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 December 21, 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.
- Do not apply
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Directions
- Wet your face with warm water before dispensing the scrub into your hands.
- Massage into your face in circular motions, focusing on areas prone to blackheads, avoiding contact with the delicate eye areas.
- Apply more or less pressure to affect the level of exfoliation and rinse away with warm water. Try not to have water too hot as this can dry your skin.
- Use 2-3 times a week and follow with your Balancing Skin Concentrate.
- Other information
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Inactive Ingredients
Aqua (Water), Cetyl Alcohol, Polysorbate 60, PPG-15 Stearyl Ether, Julgans Regia (Walnut) Shell Powder, Glycerin, Neopentyl Glycol Diisostearate, Steareth-21, Potassium Cetyl Phosphate, Triethanolamine, Xanthan Gum, Phenoxyethanol, Panthenol, Ammonium Glycyrrhizate, Disodium EDTA, Caprylyl Glycol, Ethylhexylglycerin, Bisabolol, Camellia Sinensis Leaf Extract
- Label
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INGREDIENTS AND APPEARANCE
YOURGOODSKIN BLACKHEAD CLEARING SCRUB
salicylic acid creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:68472-238 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 JUGLANS REGIA SHELL (UNII: PJ10MT7VKA) STEARETH-21 (UNII: 53J3F32P58) POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT) PHENOXYETHANOL (UNII: HIE492ZZ3T) PANTHENOL (UNII: WV9CM0O67Z) CAPRYLYL GLYCOL (UNII: 00YIU5438U) LEVOMENOL (UNII: 24WE03BX2T) CETYL ALCOHOL (UNII: 936JST6JCN) POLYSORBATE 60 (UNII: CAL22UVI4M) PPG-15 STEARYL ETHER (UNII: 1II18XLS1L) GLYCERIN (UNII: PDC6A3C0OX) NEOPENTYL GLYCOL DIISOSTEARATE (UNII: 4M6OQ34JWW) TROLAMINE (UNII: 9O3K93S3TK) XANTHAN GUM (UNII: TTV12P4NEE) AMMONIUM GLYCYRRHIZATE (UNII: 3VRD35U26C) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) GREEN TEA LEAF (UNII: W2ZU1RY8B0) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:68472-238-14 1 in 1 CARTON 03/07/2017 1 NDC:68472-238-13 125 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 03/07/2017 Labeler - BOOTS RETAIL USA INC (143151533)