Label: ACNE WARRIOR BODY WASH- salicylic acid liquid
- NDC Code(s): 61197-123-34
- Packager: Pacifica Beauty, LLC
- 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 10, 2023
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- Official Label (Printer Friendly)
- Active ingredient Purpose
- Use
- Warnings
- INDICATIONS & USAGE
- Keep out of reach of children.
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Directions
Use to cleanse face, back and other acne-prone areas every time you wash or several times a week for a deep clean. Scrub gently. Rinse thoroughly. 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. Sensitivity test for a new user. Apply product sparingly to one or two small affected areas during the first 3 days. If no discomfort occurs, follow the directions stated above.
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Inactive ingredients:
Aqua (Eau), Cocamidopropyl Betaine, Sodium C14-16 Olefin Sulfonate, Aloe Barbadensis Leaf Juice, Glycerin, Fragrance, Citric Acid, Potassium Sorbate, Sodium Benzoate, Panthenol, Allantoin, Sodium PCA, Ethylhexylglycerin, Niacinamide, Cucumis Sativus (Cucumber) Fruit Extract, Melissa Officinalis (Balm Mint) Extract, Hamamelis Virginiana (Witch Hazel) Leaf Extract.
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- Acne Warrior Body Wash Label
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INGREDIENTS AND APPEARANCE
ACNE WARRIOR BODY WASH
salicylic acid liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:61197-123 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 CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) ALLANTOIN (UNII: 344S277G0Z) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) WATER (UNII: 059QF0KO0R) SODIUM BENZOATE (UNII: OJ245FE5EU) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) CUCUMBER FRUIT OIL (UNII: R81Y52NPCT) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U) ALOE VERA LEAF (UNII: ZY81Z83H0X) GLYCERIN (UNII: PDC6A3C0OX) PANTHENOL (UNII: WV9CM0O67Z) SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2) NIACINAMIDE (UNII: 25X51I8RD4) MELISSA OFFICINALIS LEAF (UNII: 50D2ZE9219) HAMAMELIS VIRGINIANA LEAF (UNII: T07U1161SV) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:61197-123-34 355 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 02/10/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final M006 02/10/2023 Labeler - Pacifica Beauty, LLC (868275517) Establishment Name Address ID/FEI Business Operations Sun Deep Inc. 189788201 manufacture(61197-123)
