Label: 3 IN 1 CLEANSER- salicylic acid liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 72644-634-01 - Packager: SGII, 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 September 16, 2020
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredients
- Purpose
- Uses
- Warnings
- WHEN USING
- KEEP OUT OF REACH OF CHILDREN
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Directions
• Wet face. Apply one to two pumps of foam onto wet skin. Gently massage in a circular motion. Rinse well.
• 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
Water/Aqua/Eau, Decyl Glucoside, Diglycerin, Glycereth-26, PEG-6 Caprylic/Capric Glycerides, Kelp (Laminaria Digitata) Extract, Yeast (Saccharomyces Cerevisiae) Extract, Seaweed (Corallina Officinalis) Extract, Orchid (Orchis Morio) Flower Extract, Sodium Hyaluronate, Arginine, Dimethicone PEG-8 Meadowfoamate, Phenoxyethanol, Caprylyl Glycol, Ethylhexylglycerin, Fragrance/Parfum, Hexylene Glycol, Urea*, Glucosamine HCl, Propylene Glycol. *Synthetic
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
3 IN 1 CLEANSER
salicylic acid liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72644-634 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 1 g in 100 g Inactive Ingredients Ingredient Name Strength CAPRYLYL GLYCOL (UNII: 00YIU5438U) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) ARGININE (UNII: 94ZLA3W45F) FRAGRANCE CLEAN ORC0600327 (UNII: 329LCV5BTF) HEXYLENE GLYCOL (UNII: KEH0A3F75J) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) DECYL GLUCOSIDE (UNII: Z17H97EA6Y) HYALURONATE SODIUM (UNII: YSE9PPT4TH) GLUCOSAMINE HYDROCHLORIDE (UNII: 750W5330FY) UREA (UNII: 8W8T17847W) GLYCERETH-26 (UNII: NNE56F2N14) PEG-8 DIMETHICONE (UNII: GIA7T764OD) PEG-6 CAPRYLIC/CAPRIC GLYCERIDES (UNII: GO50W2HWO8) LAMINARIA DIGITATA (UNII: 15E7C67EE8) ANACAMPTIS MORIO FLOWER (UNII: PT2C4RA48D) CORALLINA OFFICINALIS (UNII: 4004498D06) WATER (UNII: 059QF0KO0R) PHENOXYETHANOL (UNII: HIE492ZZ3T) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72644-634-01 50 g in 1 BOTTLE; Type 0: Not a Combination Product 09/16/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part358H 09/16/2020 Labeler - SGII, INC. (070096792) Establishment Name Address ID/FEI Business Operations 220 LABORATORIES INC 783247950 manufacture(72644-634)
