Label: BYOMA ACNE CLEARING CLEANSER- salicylic acid liquid
- NDC Code(s): 84821-007-01
- Packager: Byoma Ltd
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated April 23, 2025
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Inactive Ingredients
Aqua (Water), Glycerin, Hamamelis Virginiana (Witch Hazel) Water, Stearic Acid, Propylene Glycol, Cocamidopropyl Betaine, Glyceryl Stearate, Sodium Methyl Cocoyl Taurate, Sodium Hydroxide, Zinc Gluconate, Glycol Distearate, Ethyl Linoleate, Phenoxyethanol, Sodium Chloride, Camellia Sinensis (Green Tea) Leaf Extract, Coconut Acid, Ethylhexylglycerin, Allantoin, Bakuchiol, Phytosphingosine, Ceramide NP, Propanediol, Rutin, Potassium Sorbate, Hydroxycinnamic Acid, Sodium Benzoate.
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INGREDIENTS AND APPEARANCE
BYOMA ACNE CLEARING CLEANSER
salicylic acid liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:84821-007 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 SODIUM BENZOATE (UNII: OJ245FE5EU) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) WATER (UNII: 059QF0KO0R) BAKUCHIOL (UNII: OT12HJU3AR) HAMAMELIS VIRGINIANA TOP WATER (UNII: NT00Y05A2V) PHYTOSPHINGOSINE (UNII: GIN46U9Q2Q) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) SODIUM HYDROXIDE (UNII: 55X04QC32I) COCONUT ACID (UNII: 40U37V505D) ETHYL LINOLEATE (UNII: MJ2YTT4J8M) GREEN TEA LEAF (UNII: W2ZU1RY8B0) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) STEARIC ACID (UNII: 4ELV7Z65AP) GLYCERIN (UNII: PDC6A3C0OX) SODIUM METHYL COCOYL TAURATE (UNII: JVL98CG53G) ZINC GLUCONATE (UNII: U6WSN5SQ1Z) PHENOXYETHANOL (UNII: HIE492ZZ3T) GLYCOL DISTEARATE (UNII: 13W7MDN21W) HYDROXYCINNAMIC ACID (UNII: IBS9D1EU3J) SODIUM CHLORIDE (UNII: 451W47IQ8X) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) ALLANTOIN (UNII: 344S277G0Z) PROPANEDIOL (UNII: 5965N8W85T) CERAMIDE NP (UNII: 4370DF050B) GLUCOMANNAN (UNII: 36W3E5TAMG) RUTIN (UNII: 5G06TVY3R7) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:84821-007-01 175 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 05/12/2025 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M006 05/12/2025 Labeler - Byoma Ltd (228554984)