X20HAIR ANTI FUNGALFOLLICULITISSHAMPOO- zinc pyrithione liquid

X20HAIR ANTI FUNGALFOLLICULITISSHAMPOO by

Drug Labeling and Warnings

X20HAIR ANTI FUNGALFOLLICULITISSHAMPOO by is a Otc medication manufactured, distributed, or labeled by Guangzhou Tata Biotechnology Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Zinc Pyrithione 1.0%

PURPOSE

Anti-dandruff

INDICATIONS & USAGE

For the relief of symptoms from scalp itch, irritationflaking, and redness associated with dandruff.

WARNINGS

For external use only

WHEN USING

Avoid contact with eyes. lf contact occurs, rinse eyesthoroughly with water.

STOP USE

If condition worsens or does not improve after regularuse of this product as directed, consult a doctor.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. lf swallowed, call a poisoncontrol center or get medical help right away.

DO NOT USE

Do not use on children under 2 years of age, unlessdirected by a doctor.

DOSAGE & ADMINISTRATION

DirectionsApply to(and coat)wet hair and scalp 3-4 times perweek (or as needed).Let sit for 2-3 minutes, then rinsewith lukewarm water.

INACTIVE INGREDIENT

Water, Sodium Laureth Sulfate, AmmoniumLauryl Sulfate,Cocamidopropyl Betaine,Dimethicone, Sodium Chloride, Phenoxyethanol.Fragrance, Sodium Benzoate, Sodium LauroylMethylaminopropionate, Butylene Glycol,Sodium Methyl Cocoyl Taurate, Triisostearin,Cocamide Mea, Guar HydroxypropyltrimoniumChloride, Sodium Taurine Cocoyl Methyltaurate,Rosmarinus Ofhcinalis(Rosemary)Leaf Oil,Camellia Sinensis Leaf Extract, GardeniaTaitensis Flower Extract,ChrysanthellumIndicum Flower Water, Aloe BarbadensisLeaf Water, Cocos Nucifera(Coconut) Oil.Disodium Edta,Glycerin, Zinc ChloridePolyquaterium-10, Etidronic Acid, Trideceth-3,Trideceth-6,Steareth-6, Sodium Polynapht-halenesulfonate, Dmdm Hydantoin, Decy!Glucoside, Cellulose Gum, Ethylhexylglycerin,Citric Acid, Squalane, Hydroxyacetophenone,Methylpropanediol, Tocopherol, HyaluronicAcid, Silanetriol.

QUESTIONS

Please call 1(213)414-8850

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

X20HAIR ANTI FUNGALFOLLICULITISSHAMPOO 
zinc pyrithione liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84066-106
Route of Administration	TOPICAL

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

Inactive Ingredients
Ingredient Name	Strength
ROSEMARY OIL (UNII: 8LGU7VM393)
TOCOPHEROL (UNII: R0ZB2556P8)
ETIDRONIC ACID (UNII: M2F465ROXU)
SODIUM METHYL COCOYL TAURATE (UNII: JVL98CG53G)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
SODIUM BENZOATE (UNII: OJ245FE5EU)
GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (UNII: B16G315W7A)
STEARETH-6 (UNII: TMO0A3Q91G)
FORMALDEHYDE/SODIUM NAPHTHALENESULFONATE COPOLYMER (3000 MW) (UNII: 90D834OZUI)
HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)
SILANETRIOL (UNII: E52D0J3TS5)
CHRYSANTHELLUM INDICUM FLOWER OIL (UNII: HJ299SUZ05)
WATER (UNII: 059QF0KO0R)
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
DIMETHICONE (UNII: 92RU3N3Y1O)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
TRIISOSTEARIN (UNII: 71503RH8KG)
FRAGRANCE LY-11285 (UNII: 6NGR43KKY9)
SODIUM TAURINE COCOYL METHYLTAURATE (UNII: B68UM74SV3)
CAMELLIA SINENSIS LEAF (UNII: W2ZU1RY8B0)
HYALURONIC ACID (UNII: S270N0TRQY)
CITRIC ACID (UNII: 2968PHW8QP)
METHYLPROPANEDIOL (UNII: N8F53B3R4R)
TRIDECETH-6 (UNII: 3T5PCR2H0C)
TRIDECETH-3 (UNII: 438A02204X)
CELLULOSE GUM (UNII: K679OBS311)
ALOE VERA LEAF OIL (UNII: JQ7YW886UQ)
ZINC CHLORIDE (UNII: 86Q357L16B)
SODIUM LAUROYL METHYLAMINOPROPIONATE (UNII: 99E3R68Y9B)
SQUALANE (UNII: GW89575KF9)
POLYQUATERNIUM-10 (400 CPS AT 2%) (UNII: HB1401PQFS)
DMDM HYDANTOIN (UNII: BYR0546TOW)
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
EDETATE DISODIUM (UNII: 7FLD91C86K)
GLYCERIN (UNII: PDC6A3C0OX)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
COCOS NUCIFERA (COCONUT) OIL (UNII: Q9L0O73W7L)
GARDENIA TAITENSIS FLOWER (UNII: T0OCU8201Y)
AMMONIUM LAURYL SULFATE (UNII: Q7AO2R1M0B)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
COCAMIDE MEA (UNII: C80684146D)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84066-106-01	300 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/27/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M032	05/20/2025

Labeler - Guangzhou Tata Biotechnology Co., Ltd. (699605102)

Registrant - Guangzhou Tata Biotechnology Co., Ltd. (699605102)