Label: VANIBISS BUTT AND THIGHS- salicylic acid cream
- NDC Code(s): 81890-002-04
- Packager: Vanibiss Inc
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated October 3, 2023
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- USE:
- WARNINGS
- STOP USE
- WHEN USING
- PREGNANCY OR BREAST FEEDING
- KEEP OUT OF REACH OF CHILDREN
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DIRECTIONS:
Clean the skin thoroughly before applying product.
Cover the entire affected area with a thin layer one to three times daily.
Because excess 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 SAFETY INFORMATION
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INACTIVE INGREDIENT
Water (Aqua), Propylene Glycol, Caprylic/Capric Triglyceride, Beeswax, Glycerin, Glyceryl Stearate, PEG-100 Stearate, Prunus Amygdalus Dulcis (Sweet Almond) Oil, Cetyl Alcohol, Organic Butyrospermum Parkii (Shea) Butter, Polyacrylamide, C13-14 Isoparaffin, Laureth-7, Caprylyl Glycol, Hexylene Glycol, Phenoxyethanol, Dimethicone, Dimethicone Crosspolymer, Polyglyceryl-6 Palmitate/Succinate, Cetearyl Alcohol, Aloe Barbadensis (Aloe Vera) Leaf Juice, Fragrance (Parfum), Sodium Hydroxide, Xanthan Gum, Disodium EDTA, Rosmarinus Officinalis (Rosemary) Extract, Tocopheryl Acetate, Mentha Piperita (Peppermint) Oil, Salix Alba Bark Extract, Camellia Sinensis Leaf Extract, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Hexyl Cinnamal, D-Limonene, Linalool, Benzyl Salicylate, Benzyl Alcohol, Citral.
- QUESTIONS
- BUTT & THIGHS ACNE TREATMENT CREAM LABEL
- BUTT & THIGHS ACNE TREATMENT CREAM BOX
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INGREDIENTS AND APPEARANCE
VANIBISS BUTT AND THIGHS
salicylic acid creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:81890-002 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 2 g in 100 mL Inactive Ingredients Ingredient Name Strength GREEN TEA LEAF (UNII: W2ZU1RY8B0) WATER (UNII: 059QF0KO0R) POLYGLYCERIN-6 (UNII: M51422LRAM) PHENOXYETHANOL (UNII: HIE492ZZ3T) DIMETHICONE/DIENE DIMETHICONE CROSSPOLYMER (UNII: RSA9I561OK) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) ALMOND OIL (UNII: 66YXD4DKO9) CETYL ALCOHOL (UNII: 936JST6JCN) SHEA BUTTER (UNII: K49155WL9Y) XANTHAN GUM (UNII: TTV12P4NEE) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) LAURETH-7 (UNII: Z95S6G8201) GLYCERIN (UNII: PDC6A3C0OX) CAPRYLYL GLYCOL (UNII: 00YIU5438U) EDETATE DISODIUM (UNII: 7FLD91C86K) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) C13-14 ISOPARAFFIN (UNII: E4F12ROE70) HEXYLENE GLYCOL (UNII: KEH0A3F75J) LIMONENE, (+)- (UNII: GFD7C86Q1W) ALOE VERA LEAF (UNII: ZY81Z83H0X) TEA TREE OIL (UNII: VIF565UC2G) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) WHITE WAX (UNII: 7G1J5DA97F) GLYCERYL STEARATE/PEG-100 STEARATE (UNII: RD25J5V947) SODIUM HYDROXIDE (UNII: 55X04QC32I) ROSEMARY (UNII: IJ67X351P9) PEPPERMINT OIL (UNII: AV092KU4JH) .ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I) LINALOOL, (+/-)- (UNII: D81QY6I88E) BENZYL SALICYLATE (UNII: WAO5MNK9TU) BENZYL ALCOHOL (UNII: LKG8494WBH) CITRAL (UNII: T7EU0O9VPP) SALIX ALBA BARK (UNII: 205MXS71H7) Product Characteristics Color white Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:81890-002-04 1 in 1 BOX 11/02/2023 1 118 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 Drug M006 11/02/2023 Labeler - Vanibiss Inc (104730560)