Label: SLMD SALICYLIC ACID BODY WASH- salicylic acid liquid
- NDC Code(s): 59958-405-01, 59958-405-02
- Packager: Owen Biosciences 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 January 16, 2023
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredients
- Use
- Warnings For external use only
- Keep out of reach of children.
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Directions
• use daily.
• apply to wet hands and create a lather.
• massage over wet skin concentrating on
areas prone to breakouts.
• rinse thoroughly with warm water.
• for best results use with SLMD Acne Body Spray.
• 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. - Other information
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Inactive Ingredients
Water, Cocamidopropyl Betaine, Disodium Laureth Sulfosuccinate, Coco-Betaine, Glycerin, Aloe Barbadensis Leaf Extract, Lauric Acid, Lactobacillus/Saccharomyces/Rice/Sucrose Ferment Filtrate, Beta-glucan, Hydroxyphenyl Propamidobenzoic Acid, Lactic Acid, Panthenol, Allantion, Myristoyl Tetrapeptide-13, Eucalyptus Globulus Leaf Oil, Retinyl Palmitate, Oligopeptide-8, Tocopheryl Acetate, Simmodsia Chinensis (Jojoba) Seed Oil, Butylene Glycol, Disodium EDTA, Xanthan Gum, Phenoxyethanol, Caprylyl Glycol, Pentylene Glycol.
- Use
- SA Body Wash.jpg
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INGREDIENTS AND APPEARANCE
SLMD SALICYLIC ACID BODY WASH
salicylic acid liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:59958-405 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 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) 58.25 g in 100 g COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) 8.8 g in 100 g DISODIUM LAURETH SULFOSUCCINATE (UNII: D6DH1DTN7E) 8.5 g in 100 g GLYCERIN (UNII: PDC6A3C0OX) 5 g in 100 g Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:59958-405-02 1 in 1 CARTON 08/30/2019 1 NDC:59958-405-01 240 g 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 08/30/2019 Labeler - Owen Biosciences Inc. (790003045) Registrant - Owen Biosciences Inc. (790003045) Establishment Name Address ID/FEI Business Operations Owen Biosciences Inc. 790003045 manufacture(59958-405)