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-dandruf

INDICATIONS & USAGE

helps prevent recurence of flaking and itchlngassoclated wlth dandnrff

WARNINGS

For oxternal use only.

DO NOT USE

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

WHEN USING

you have a condition that covers a large areaof the bady.

STOP USE

condition worsens or does not imprve afterregular use of this prpduct as directed.
Iritation, dryness, or an allerglc reactlon occur8and consult a healthcare professlonal.

KEEP OUT OF REACH OF CHILDREN

get medical help or contact a Poison ContolCenter right away.

DOSAGE & ADMINISTRATION

for best results, use at least twlce a week or asdirected by a doctor.
for maxirnum dandnrff contrl, use every timeyou shampoo.
shake before use
wet hair, massage onto scalp, rinse, repeat ifdeslred.

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
blue 1 CI 42090

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ANTI DANDRUFF SHAMPOOS 
pyrithione zinc liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85434-001
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
SODIUM CHLORIDE (UNII: 451W47IQ8X)
ZINC CHLORIDE (UNII: 86Q357L16B)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
TRIDECETH-10 (UNII: G624N6MSBA)
WATER (UNII: 059QF0KO0R)
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
PRUNUS PERSICA LEAF (UNII: VN3501T41P)
ALOE BARBADENSIS LEAF POWDER (UNII: ZY81Z83H0X)
AMMONIUM LAURYL SULFATE (UNII: Q7AO2R1M0B)
FRAGRANCE 13576 (UNII: 5EM498GW35)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
SODIUM BENZOATE (UNII: OJ245FE5EU)
DIMETHICONE (UNII: 92RU3N3Y1O)
CITRIC ACID (UNII: 2968PHW8QP)
GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (UNII: B16G315W7A)
ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S) (UNII: 8Z5ZAL5H3V)
TRIDECETH-3 (UNII: 438A02204X)
TREHALOSE (UNII: B8WCK70T7I)
CI 42090 (UNII: H3R47K3TBD)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85434-001-01	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(85434-001)