ANTI DANDRUFF SHAMPOOS- pyrithione zinc liquid

anti dandruff SHAMPOOS by

Drug Labeling and Warnings

anti dandruff SHAMPOOS by is a Otc medication manufactured, distributed, or labeled by Guangdong Quaker Daily Chemical Co., LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Pyrithione zinc 1%

PURPOSE

Anti-dandruff

INDICATIONS & USAGE

helps prevent recurence of flaking and itchingassociated with dandruff

WARNINGS

For external uae only.

DO NOT USE

in eyes and mucous membranes. lf contactoccurs, rinse thoroughly with water.

WHEN USING

you have a conditon that covers a large area of the body.

STOP USE

condltlan worsens or does not lmprove afterregular use of thls product as dlrected.
iritation, dryness, or an allergic reaction occursand consult a healtheare professional.

KEEP OUT OF REACH OF CHILDREN

Keep out of roach of chlldren. lf swallowed.get medlcal help or contact a Pokson ControlCanter rlght away

DOSAGE & ADMINISTRATION

for best results, use at least twice a week or asdirectad by a doctor.
for maxmum dandruff control, use every tmeyou shampoo
shake before use.
wet halr, massage onto scalp, rinse, repeat lf desired.

INACTIVE INGREDIENT

water
sodium laureth sulfate
cocamidopropyl betaine
guar hydroxypropyltrimonium chloride
acrylates/c10-30 alkyl acrylate crosspolymer
zinc chloride
sodium chloride
methylchloroisothiazolinone
dimethicone
trideceth-3
trideceth-10
citric acid
prunus persica (peach) leaf extract
trehalose
aloe barbadensis leaf juice
ammonium lauryl sulfate
sodium benzoate
fragrance

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ANTI DANDRUFF SHAMPOOS 
pyrithione zinc liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85434-002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PYRITHIONE ZINC (UNII: R953O2RHZ5) (PYRITHIONE ZINC - UNII:R953O2RHZ5)	PYRITHIONE ZINC	1 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
FRAGRANCE 13576 (UNII: 5EM498GW35)
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
AMMONIUM LAURYL SULFATE (UNII: Q7AO2R1M0B)
PRUNUS PERSICA LEAF (UNII: VN3501T41P)
TREHALOSE (UNII: B8WCK70T7I)
GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (UNII: B16G315W7A)
ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S) (UNII: 8Z5ZAL5H3V)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
SODIUM BENZOATE (UNII: OJ245FE5EU)
ALOE BARBADENSIS LEAF POWDER (UNII: ZY81Z83H0X)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
TRIDECETH-10 (UNII: G624N6MSBA)
CITRIC ACID (UNII: 2968PHW8QP)
TRIDECETH-3 (UNII: 438A02204X)
DIMETHICONE (UNII: 92RU3N3Y1O)
WATER (UNII: 059QF0KO0R)
ZINC CHLORIDE (UNII: 86Q357L16B)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85434-002-01	1 in 1 BOX	03/26/2025
1		473 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M032	03/26/2025

Labeler - Guangdong Quaker Daily Chemical Co., LTD (548075342)

Establishment
Name	Address	ID/FEI	Business Operations
Guangdong Quaker Daily Chemical Co., LTD		548075342	manufacture(85434-002)