Label: ANTI DANDRUFF- ketoconazole liquid
- NDC Code(s): 74458-157-01
- Packager: Guangzhou Yilong Cosmetics.,Ltd
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated July 4, 2026
If you are a consumer or patient please visit this version.
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INDICATIONS & USAGE
DIRECTIONS FOR USE
For best results, follow these stepscarefully:
1.Wet hair and scalp thoroughly with
lukewarm water.
2.Applya sufficient amountof shampoo to
generate a rich lather.
3.Gently massage the lather into your scalp
and hair.
4.Leave the lather on the scalpfor3-5minutes. This contact time is crucialforthemedication to work effectively.5.Rinse thoroughly with water. -
WARNINGS
PRECAUTIONS
For externaluse only.Avoid contact witheyes. Ifcontactoccurs, rinse thoroughlywithwater.Stop use and consult a doctor if youexperience severe irritation, rash, oranysigns of an allergic reaction (e.g., swelling,dizziness, trouble breathing). Before usingthis shampoo if you have known allergiesto ketoconazole or any other ingredients. -
INACTIVE INGREDIENT
Aqua
Sodium Laureth Sulfate
Cocamide DEA
Sodium Chloride
Cocamidopropyl Betaine
Ammonium Lauryl Sulfate
Fragrance
Phenoxyethanol
PEG-7 Glyceryl Cocoate
Bis-Aminopropyl Dimethicone
Hydroxypropyl Guar
Hydroxypropyltrimonium Chloride
C12-13 Pareth Lactate
Citric Acid
C11-15 Pareth-9
Trideceth-12
Sodium Benzoate - PURPOSE
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
ANTI DANDRUFF
ketoconazole liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:74458-157 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength KETOCONAZOLE (UNII: R9400W927I) (KETOCONAZOLE - UNII:R9400W927I) KETOCONAZOLE 1 mg in 100 mg Inactive Ingredients Ingredient Name Strength AQUA (UNII: 059QF0KO0R) 50 mg in 100 mg Product Characteristics Color Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:74458-157-01 200 mg in 1 BOTTLE; Type 0: Not a Combination Product 07/04/2026 
Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M032 07/04/2026 Labeler - Guangzhou Yilong Cosmetics.,Ltd (420929116) Registrant - Guangzhou Yilong Cosmetics.,Ltd (420929116)

