Label: VANIBISS BUTT AND THIGHS ACNE TREATMENT CREAM- salicylic acid cream
- NDC Code(s): 81890-192-00
- Packager: Vanibiss Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 11, 2023
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- Official Label (Printer Friendly)
- Drug Facts
- Active ingredients
- Uses
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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. If irritation occurs, only use one topical acne medication at a time.
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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 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:
Aloe Barbadensis Leaf (Aloe Vera Gel) Juice, Aqua (Deionized Water), Ascorbic Acid (Vitamin C), Beeswax, Bis-Vinyl Dimethicone/Dimethicone Copolymer, Butyrospermum Parkii (Shea) Butter, Camellia Sinensis (Green Tea) Extract, Caprylic/Capric Triglyceride, Caprylyl Glycol, Carthamus Tinctorius (Safflower) Oil, Centella Asiatica (Gotu Kola) Extarct, Cetearyl Alcohol, Cetearyl Glucoside, Cetearyl Olivate, Cetyl Alcohol, Citric Acid, Cyclopentasiloxane, Glyceryl Stearate, Glycyrrhiza Glabra (Licorice) Extract, Hamamelis Virginiana (Witch Hazel) Distillate, Hydroxyethyl Acrylate/Sodium (Flax) Seed Oil, Mentha Piperita (Peppermint) Oil, Parfum (Fragrance), Phenoxyethanol, Polysorbate-20, Rosmarinus Officinalis (Rosemary) Extarct, Salix Alba (Willow) Bark Extarct, Sodium Hydroxide, Sorbitan Olivate, Tetrasodium EDTA, Thymus Vulgaris (Thyme) Extarct, Zemea (Corn) propanediol, Zinc Oxide.
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INGREDIENTS AND APPEARANCE
VANIBISS BUTT AND THIGHS ACNE TREATMENT CREAM
salicylic acid creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:81890-192 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 ALOE VERA LEAF (UNII: ZY81Z83H0X) WATER (UNII: 059QF0KO0R) ASCORBIC ACID (UNII: PQ6CK8PD0R) YELLOW WAX (UNII: 2ZA36H0S2V) SHEA BUTTER (UNII: K49155WL9Y) GREEN TEA LEAF (UNII: W2ZU1RY8B0) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) CAPRYLYL GLYCOL (UNII: 00YIU5438U) SAFFLOWER (UNII: 4VBL71TY4Y) CENTELLA ASIATICA LEAF (UNII: 6810070TYD) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) CETEARYL GLUCOSIDE (UNII: 09FUA47KNA) CETEARYL OLIVATE (UNII: 58B69Q84JO) CETYL ALCOHOL (UNII: 936JST6JCN) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) GLYCYRRHIZA GLABRA (UNII: 2788Z9758H) HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK (UNII: T7S323PKJS) LINSEED OIL (UNII: 84XB4DV00W) PEPPERMINT OIL (UNII: AV092KU4JH) PHENOXYETHANOL (UNII: HIE492ZZ3T) POLYSORBATE 20 (UNII: 7T1F30V5YH) ROSEMARY (UNII: IJ67X351P9) SALIX ALBA BARK (UNII: 205MXS71H7) SODIUM HYDROXIDE (UNII: 55X04QC32I) SORBITAN OLIVATE (UNII: MDL271E3GR) EDETATE SODIUM (UNII: MP1J8420LU) THYME (UNII: CW657OBU4N) CORN (UNII: 0N8672707O) ZINC OXIDE (UNII: SOI2LOH54Z) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:81890-192-00 1 in 1 BOX 05/10/2021 1 118.3 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 05/10/2021 Labeler - Vanibiss Inc (104730560)
