Label: BAREMINERALS BLEMISH REMEDY ACNE TREATMENT GELEE CLEANSER- salicylic acid emulsion
- NDC Code(s): 98132-770-01
- Packager: Orveon Global US LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 22, 2024
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- SPL UNCLASSIFIED SECTION
- Active ingredient(s)
- Purpose
- Use
- Warnings
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Directions
- cover the entire affected area with a thin layer of product and rinse thoroughly one to three times daily
- because excessive drying out 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
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Inactive ingredients
water (aqua/eau), sorbitol, cocamidopropyl betaine, sodium lauryl glycol carboxylate, glycerin, disodium edta, cinnamomum zeylanicum bark extract, mentha piperita (peppermint) leaf extract, zingiber officinale (ginger) root extract, sea salt, fragrance (parfum), limonene, sodium benzoate, phenoxyethanol.
- Questions or comments?
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 120 g Tube Carton
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INGREDIENTS AND APPEARANCE
BAREMINERALS BLEMISH REMEDY ACNE TREATMENT GELEE CLEANSER
salicylic acid emulsionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:98132-770 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 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) SORBITOL (UNII: 506T60A25R) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) SODIUM LAURYL GLYCOL CARBOXYLATE (UNII: 8L0472VMYL) GLYCERIN (UNII: PDC6A3C0OX) EDETATE DISODIUM (UNII: 7FLD91C86K) CINNAMON BARK OIL (UNII: XE54U569EC) MENTHA PIPERITA LEAF (UNII: A389O33LX6) GINGER (UNII: C5529G5JPQ) SEA SALT (UNII: 87GE52P74G) LIMONENE, (+/-)- (UNII: 9MC3I34447) SODIUM BENZOATE (UNII: OJ245FE5EU) PHENOXYETHANOL (UNII: HIE492ZZ3T) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:98132-770-01 1 in 1 CARTON 01/30/2016 1 120 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 Drug M006 01/30/2016 Labeler - Orveon Global US LLC (118344494)