Label: STAGE FIGHT ACNE MASK- sulfur, resorcinol paste
- NDC Code(s): 49825-137-01, 49825-137-02
- Packager: Bioelements, Inc
- This is a repackaged label.
- Source NDC Code(s): 56152-0254
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated September 10, 2024
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
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WARNINGS
Warnings
for external use only.
when using this product: skin irritation and dryness is more likely to occur if you use another topical acne medication at the same time. rinse right away with water if it gets in eyes.
do not use on broken skin or large areas of the skin. when using this product apply only to areas with acne.
- DOSAGE & ADMINISTRATION
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INACTIVE INGREDIENT
inactive ingredients
Water (Aqua, Eau), Kaolin, Glycerin, Decyl Glucoside, Caprylic/Capric Triglyceride, Cetyl Alcohol, Stearyl Alcohol, Titanium Dioxide, Niacinamide, Lactic Acid, Centella Asiatica Extract, Lavandula Angustifolia (Lavender) Flower/Leaf/Stem Extract, Thymus Vulgaris (Thyme) Extract, Hibiscus Sabdariffa Flower Extract, Origanum Vulgare (Oregano) Leaf Oil, Bisabolol, Olea Europaea (Oliva) Fruit Oil, Magnesium Aluminum Silicate, Polyacrylate Crosspolymer-6, Xantham Gum, Phenoxyethanol, Sodium Citrate, Citric Acid
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
STAGE FIGHT ACNE MASK
sulfur, resorcinol pasteProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49825-137(NDC:56152-0254) Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70) SULFUR 8 g in 100 mL RESORCINOL (UNII: YUL4LO94HK) (RESORCINOL - UNII:YUL4LO94HK) RESORCINOL 2 g in 100 mL Inactive Ingredients Ingredient Name Strength KAOLIN (UNII: 24H4NWX5CO) SODIUM CITRATE (UNII: 1Q73Q2JULR) OLIVE OIL (UNII: 6UYK2W1W1E) THYME (UNII: CW657OBU4N) CENTELLA ASIATICA TRITERPENOIDS (UNII: 4YS74Q4G4J) OREGANO LEAF OIL (UNII: 7D0CGR40U1) MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC) XANTHAN GUM (UNII: TTV12P4NEE) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) GLYCERIN (UNII: PDC6A3C0OX) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) STEARYL ALCOHOL (UNII: 2KR89I4H1Y) LACTIC ACID (UNII: 33X04XA5AT) HIBISCUS SABDARIFFA FLOWER (UNII: 45TGG6IU6M) AMMONIUM ACRYLOYLDIMETHYLTAURATE, DIMETHYLACRYLAMIDE, LAURYL METHACRYLATE AND LAURETH-4 METHACRYLATE COPOLYMER, TRIMETHYLOLPROPANE TRIACRYLATE CROSSLINKED (45000 MPA.S) (UNII: Q7UI015FF9) PHENOXYETHANOL (UNII: HIE492ZZ3T) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) CETYL ALCOHOL (UNII: 936JST6JCN) LAVANDULA ANGUSTIFOLIA SUBSP. ANGUSTIFOLIA FLOWERING TOP (UNII: 9YT4B71U8P) WATER (UNII: 059QF0KO0R) LEVOMENOL (UNII: 24WE03BX2T) DECYL GLUCOSIDE (UNII: Z17H97EA6Y) NIACINAMIDE (UNII: 25X51I8RD4) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49825-137-02 1 in 1 CARTON 09/01/2024 1 NDC:49825-137-01 118 mL in 1 JAR; 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 09/01/2024 Labeler - Bioelements, Inc (174813923)
