Label: BAREMINERALS BLEMISH REMEDY ACNE CLEARING TREATMENT SERUM- salicylic acid emulsion
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Contains inactivated NDC Code(s)
NDC Code(s): 98132-771-01 - Packager: Bare Escentuals Beauty, 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 May 12, 2016
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- Official Label (Printer Friendly)
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- Active ingredient(s)
- Purpose
- Use
- Warnings
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Directions
- clean skin thoroughly before applying this product
- cover the entire affected area with a thin layer of product 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), butylene glycol, glycerin, peg-32, peg-6, peg-8, sodium lactate, zinc pca, potassium hydroxide, peg/ppg-17/4 dimethyl ether, urea, glucosamine hcl, algae extract, saccharomyces cerevisiae extract, hydrogenated dimer dilinoleyl peg-44/poly(1,2-butanediol)-15 dimethyl ether, ethylhexylglycerin, xanthan gum, trehalose, spiraea ulmaria extract, dipotassium glycyrrhizate, alcohol , disodium edta, paeonia suffruticosa root extract, tocopherol, fragrance (parfum), limonene, phenoxyethanol.
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- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 30 ml Bottle Carton
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INGREDIENTS AND APPEARANCE
BAREMINERALS BLEMISH REMEDY ACNE CLEARING TREATMENT SERUM
salicylic acid emulsionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:98132-771 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 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) GLYCERIN (UNII: PDC6A3C0OX) POLYETHYLENE GLYCOL 1500 (UNII: 1212Z7S33A) POLYETHYLENE GLYCOL 300 (UNII: 5655G9Y8AQ) POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) SODIUM LACTATE (UNII: TU7HW0W0QT) ZINC PIDOLATE (UNII: C32PQ86DH4) POTASSIUM HYDROXIDE (UNII: WZH3C48M4T) PEG/PPG-17/4 DIMETHYL ETHER (UNII: 4ET18WJG5K) UREA (UNII: 8W8T17847W) GLUCOSAMINE HYDROCHLORIDE (UNII: 750W5330FY) SACCHAROMYCES CEREVISIAE (UNII: 978D8U419H) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) XANTHAN GUM (UNII: TTV12P4NEE) TREHALOSE (UNII: B8WCK70T7I) GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX) ALCOHOL (UNII: 3K9958V90M) EDETATE DISODIUM (UNII: 7FLD91C86K) PAEONIA SUFFRUTICOSA ROOT (UNII: 7M7E9A2C8J) TOCOPHEROL (UNII: R0ZB2556P8) LIMONENE, (+/-)- (UNII: 9MC3I34447) PHENOXYETHANOL (UNII: HIE492ZZ3T) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:98132-771-01 1 in 1 CARTON 01/01/2017 1 30 mL in 1 BOTTLE, GLASS; 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 01/01/2017 Labeler - Bare Escentuals Beauty, Inc. (087008363)