Label: SUGAR RUSH NO BULLZIT ACNE SPOT TREATMENT- salicylic acid liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 51060-227-01 - Packager: Tarte, 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 February 6, 2020
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredients
- Purpose
- Uses
- Warnings
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Directions
- Clean the skin thoroughly before applying this product.
- Cover the entire affected area with a thin layer one to three times a daily.
- 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, SD alcohol 40-B, butylene glycol, niacinamide, carbomer, octadecenedioic acid, phenoxyethanol, aminomethyl propanol, azelaic acid, caffeine, sodium ascorbyl phosphate, glycerin, hamamelis virginiana (witch hazel) extract, eugenia caryophyllus (clove) leaf oil, eugenol, cucumis sativus (cucumber) fruit extract, origanum vulgare leaf oil. DX110AT000011.
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 10 mL Tube Carton
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INGREDIENTS AND APPEARANCE
SUGAR RUSH NO BULLZIT ACNE SPOT TREATMENT
salicylic acid liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:51060-227 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 15 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) NIACINAMIDE (UNII: 25X51I8RD4) CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC) OCTADECENEDIOIC ACID (UNII: 565ZMT5QRG) PHENOXYETHANOL (UNII: HIE492ZZ3T) AMINOMETHYLPROPANOL (UNII: LU49E6626Q) AZELAIC ACID (UNII: F2VW3D43YT) CAFFEINE (UNII: 3G6A5W338E) SODIUM ASCORBYL PHOSPHATE (UNII: 836SJG51DR) GLYCERIN (UNII: PDC6A3C0OX) HAMAMELIS VIRGINIANA TOP (UNII: UDA30A2JJY) CLOVE LEAF OIL (UNII: VCA5491KVF) EUGENOL (UNII: 3T8H1794QW) CUCUMBER (UNII: YY7C30VXJT) OREGANO LEAF OIL (UNII: 7D0CGR40U1) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:51060-227-01 1 in 1 CARTON 08/14/2019 1 10 mL 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 08/14/2019 Labeler - Tarte, Inc. (027905186)