SELENIUMDISULFIDEANTI-DANDRUFFSHAMPOO- selenium disulfide anti-dandruff shampoo liquid

SELENIUMDISULFIDEANTI-DANDRUFFSHAMPOO by

Drug Labeling and Warnings

SELENIUMDISULFIDEANTI-DANDRUFFSHAMPOO by is a Otc medication manufactured, distributed, or labeled by Guangzhou Yixin Cross-border E-commerce Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredients

Selenium disulfide 1%

Purpose

Antidandruff agent

Uses:

Treats and prevents dandruff
Controls flaking and itching of the scalp

Warnings

For external use only.

Flammable: Keep away from fire or flame

Dosage and administration

​Adults and children 3 years and older:​​

Wet hair thoroughly
Apply amount to cover scalp (approx. 1 teaspoon)
Massage 3-5 minutes until lather forms
Rinse completely with water
Repeat twice weekly

Children under 3 years:​​ Do not use

Do NOT use:

On broken or inflamed skin
In children under 3 years
If allergic to selenium compounds

When using this product:

Avoid contact with eyes (if occurs, rinse immediately)
Discontinue use if vision changes occur

Stop use and ask a doctor if:​

Skin irritation or rash occurs
Condition worsens or persists after 8 weeks

Keep out of reach of children.

Keep out of reach of children.​

Inactive ingredients

Water, Ammonium Lauryl Sulfate, Citric Acid, Sea Salt, Phenoxyethanol, Tocopherols

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

SELENIUMDISULFIDEANTI-DANDRUFFSHAMPOO 
selenium disulfide anti-dandruff shampoo liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84778-080
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SELENIUM SULFIDE (UNII: Z69D9E381Q) (SELENIUM SULFIDE - UNII:Z69D9E381Q)	SELENIUM SULFIDE	1 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
TOCOPHEROL (UNII: R0ZB2556P8)
AMMONIUM LAURYL SULFATE (UNII: Q7AO2R1M0B)
WATER (UNII: 059QF0KO0R)
SEA SALT (UNII: 87GE52P74G)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
CITRIC ACID (UNII: 2968PHW8QP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84778-080-01	300 g in 1 BOTTLE; Type 0: Not a Combination Product	08/26/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M032	08/26/2025

Labeler - Guangzhou Yixin Cross-border E-commerce Co., Ltd. (455800881)

Establishment
Name	Address	ID/FEI	Business Operations
Guangzhou Yixin Cross-border E-commerce Co., Ltd.		455800881	label(84778-080) , manufacture(84778-080)