Label: PERT 2 IN 1 EXTRA STRENGTH- salicylic acid shampoo
- NDC Code(s): 81277-803-12
- Packager: Sodalis USA, LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 31, 2024
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- Drug Facts
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- DOSAGE & ADMINISTRATION
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INACTIVE INGREDIENT
Inactive ingredients: Water (aqua), sodium laureth sulfate, sodium lauryl sulfate, cocamidopropyl betaine, glycerin, cocamide MEA, dimethicone, glycol distearate, fragrance (parfum), guar hydroxypropyltrimonium chloride, sodium citrate, acrylates/C10-30 alkyl acrylate crosspolymer, sodium benzoate, sodium chloride, methylchloroisothiazolinone, methylisothiazolinone, sodium hydroxide, D-limonene, linalool, FD&C Yellow no. 10, FD&C Blue no. 1
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INGREDIENTS AND APPEARANCE
PERT 2 IN 1 EXTRA STRENGTH
salicylic acid shampooProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:81277-803 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 3 g in 100 mL Inactive Ingredients Ingredient Name Strength LINALOOL (UNII: D81QY6I88E) LIMONENE, (+)- (UNII: GFD7C86Q1W) GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (1.7 SUBSTITUENTS PER SACCHARIDE) (UNII: B16G315W7A) ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S) (UNII: 8Z5ZAL5H3V) GLYCERIN (UNII: PDC6A3C0OX) COCO MONOETHANOLAMIDE (UNII: C80684146D) GLYCOL DISTEARATE (UNII: 13W7MDN21W) SODIUM CITRATE (UNII: 1Q73Q2JULR) WATER (UNII: 059QF0KO0R) DIMETHICONE (UNII: 92RU3N3Y1O) SODIUM BENZOATE (UNII: OJ245FE5EU) SODIUM CHLORIDE (UNII: 451W47IQ8X) D&C YELLOW NO. 10 (UNII: 35SW5USQ3G) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) SODIUM LAURETH SULFATE (UNII: BPV390UAP0) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) SODIUM LAURYL SULFATE (UNII: 368GB5141J) METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:81277-803-12 355 mL in 1 BOTTLE; Type 0: Not a Combination Product 11/18/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M032 11/18/2024 Labeler - Sodalis USA, LLC (119375257)