ANTI-DANDRUFF- anti-dandruff shampoo shampoo

Anti-Dandruff by

Drug Labeling and Warnings

Anti-Dandruff by is a Otc medication manufactured, distributed, or labeled by Shenzhen Derbit Technology Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

ZINC PYRITHION (0.384%)

AMMONIUM LAURYL SULFATE (3.22%)

purpose

Anti-dandruff

Detergent

use

Wet your hair first, then pour the shampoo into your hands, rub it and use it on your hair

Warning

If shampoo accidentally gets into your eyes, rinse your eyes immediately with water，If your scalp feels uncomfortable after use, please stop using it immediately

Do not use

Please do not use if you are allergic or itchy after use.

When using SECTION

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

OTC-STOP USE SECTION

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Direction

n/a

STORAGE AND HANDLING

n/a

inactive ingredients

CAMELLIA JAPONICA SEED OIL

CAMELLIA SINENSIS LEAF EXTRACT

GLYCERIN

GLEDITSIA SINENSIS EXTRACT

HYDROGENATED CASTOR OIL

WATER

ZINGIBER OFFICINALE EXTRACT

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ANTI-DANDRUFF 
anti-dandruff shampoo shampoo

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83619-002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PYRITHIONE ZINC (UNII: R953O2RHZ5) (PYRITHIONE ZINC - UNII:R953O2RHZ5)	PYRITHIONE ZINC	0.384 g  in 100 mL
AMMONIUM LAURYL SULFATE (UNII: Q7AO2R1M0B) (AMMONIUM CATION - UNII:54S68520I4)	AMMONIUM CATION	3.22 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
CAMELLIA JAPONICA SEED OIL (UNII: U37N0S910T)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
GREEN TEA LEAF (UNII: W2ZU1RY8B0)
HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)
GINGER (UNII: C5529G5JPQ)
GLEDITSIA SINENSIS WHOLE (UNII: FS3UB95UTG)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83619-002-01	250 mL in 1 BOX; Type 0: Not a Combination Product	01/04/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M032	01/04/2024

Labeler - Shenzhen Derbit Technology Co., Ltd. (540583392)

Establishment
Name	Address	ID/FEI	Business Operations
Shenzhen Derbit Technology Co., Ltd.		540583392	manufacture(83619-002)