Label: AEWAJIN HASUOSHAMPOO- menthol, salicylic acid, panthenol shampoo
- NDC Code(s): 73466-0007-1
- Packager: MISOCOS
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.
Drug Label Information
Updated January 2, 2022
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- WARNINGS
- DOSAGE & ADMINISTRATION
-
INACTIVE INGREDIENT
Water, Sodium Lauryl Sulfate, Sodium Laureth Sulfate, Camellia Sinensis Leaf/Ficus Carica (Fig) Leaf/Morus Alba
Leaf/Root Extract, Sodium Chloride, Cocamidopropyl Betaine, Polygonum Multiflorum Root Extract, Butylene
Glycol, Diospyros Kaki Fruit Extract, Camellia Japonica Leaf Extract, Ceratonia Siliqua (Carob) Fruit Extract, 1,2-
Hexanediol, Glycol Distearate, Cocamide MEA, Dimethicone, L-Menthol, Salicylic Acid, Dexpanthenol, Sodium
Citrate, Polyquaternium-10, Polyquaternium-7, Disodium EDTA, Caramel, Phenoxyethanol, Laureth-3, Sodium
Benzoate, Guar Hydroxypropyltrimonium Chloride, Fragrance, Benzyl Alcohol - INDICATIONS & USAGE
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
AEWAJIN HASUOSHAMPOO
menthol, salicylic acid, panthenol shampooProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73466-0007 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 0.25 g in 100 mL MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 0.3 g in 100 mL PANTHENOL (UNII: WV9CM0O67Z) (PANTHENOL - UNII:WV9CM0O67Z) PANTHENOL 0.2 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73466-0007-1 500 mL in 1 BOTTLE; Type 0: Not a Combination Product 01/02/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 01/02/2022 Labeler - MISOCOS (695640173) Registrant - MISOCOS (695640173) Establishment Name Address ID/FEI Business Operations MISOCOS 695640173 manufacture(73466-0007)