Label: PIMPLE POTION RETINAL PLUS SALICYLIC ACID ACNE TREATMENT- salicylic acid cream
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Contains inactivated NDC Code(s)
NDC Code(s): 62742-4182-1, 62742-4182-2 - Packager: Allure Labs 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 12, 2019
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- DO NOT USE
- KEEP OUT OF REACH OF CHILDREN
- WHEN USING
- STOP USE
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DOSAGE & ADMINISTRATION
- Clean the skin thoroughly before applying this 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 to 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 SAFETY INFORMATION
- QUESTIONS
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INACTIVE INGREDIENT
Water (Aqua), Caprylic/Capric Triglyceride, Cetearyl Alcohol, Sorbitan Stearate, Glycerin, Cetyl Ethylhexanoate, Glyceryl Stearate, Lactobacillus Ferment, Retinal, Bakuchiol, Persea Gratissima (Avocado) Oil, Centella Asiatica Extract, Daucus Carota Sativa (Carrrot) Root Extract, Citrus Aurantium Dulcis (Orange) Peel Oil, Lavandula Angustifolia (Lavender) Oil, Litsea Cubeba fruit Oil, Rosmarinus Officinalis (Rosemary) Leaf Oil, Cananga Odorata Flower Oil, Xanthan Gum, Polyacrylate Crosspolymer-6, Phenoxyethanol, Ethylhexylglycerin, Sodium Phytate.
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
PIMPLE POTION RETINAL PLUS SALICYLIC ACID ACNE TREATMENT
salicylic acid creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:62742-4182 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 20 mg in 1 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X) GLYCERIN (UNII: PDC6A3C0OX) CETYL ETHYLHEXANOATE (UNII: 134647WMX4) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) LACTOBACILLUS REUTERI (UNII: 9913I24QEE) RETINAL, ALL-TRANS (UNII: RR725D715M) BAKUCHIOL (UNII: OT12HJU3AR) AVOCADO OIL (UNII: 6VNO72PFC1) CENTELLA ASIATICA WHOLE (UNII: 7M867G6T1U) CARROT (UNII: L56Z1JK48B) ORANGE OIL (UNII: AKN3KSD11B) LAVENDER OIL (UNII: ZBP1YXW0H8) LITSEA OIL (UNII: 2XIW34BN6O) ROSEMARY OIL (UNII: 8LGU7VM393) CANANGA OIL (UNII: 8YOY78GNNX) XANTHAN GUM (UNII: TTV12P4NEE) AMMONIUM ACRYLOYLDIMETHYLTAURATE, DIMETHYLACRYLAMIDE, LAURYL METHACRYLATE AND LAURETH-4 METHACRYLATE COPOLYMER, TRIMETHYLOLPROPANE TRIACRYLATE CROSSLINKED (45000 MPA.S) (UNII: Q7UI015FF9) PHENOXYETHANOL (UNII: HIE492ZZ3T) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) PHYTATE SODIUM (UNII: 88496G1ERL) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:62742-4182-2 1 in 1 CARTON 12/12/2019 1 NDC:62742-4182-1 15 g 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 12/12/2019 Labeler - Allure Labs Inc (926831603)