KERASTASE PARIS SYMBIOSE ANTIDANDRUFF- pyrithione zinc shampoo

Country: United States

Language: English

Source: NLM (National Library of Medicine)

Active ingredient:

PYRITHIONE ZINC (UNII: R953O2RHZ5) (PYRITHIONE ZINC - UNII:R953O2RHZ5)

Available from:

L'Oreal USA Products Inc

Administration route:

TOPICAL

Prescription type:

OTC DRUG

Therapeutic indications:

Antidandruff - helps eliminate the symptoms of dandruff condition worsens or does not improve after regular use of this product as directed

Authorization status:

OTC monograph final

Summary of Product characteristics

KERASTASE PARIS SYMBIOSE ANTIDANDRUFF- PYRITHIONE ZINC SHAMPOO
L'OREAL USA PRODUCTS INC
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DRUG FACTS
ACTIVE INGREDIENT
Pyrithione zinc 1%
PURPOSE
Antidandruff
USES
helps eliminate the symptoms of dandruff
WARNINGS
For external use only
WHEN USING THIS PRODUCT
avoid contact with the eyes. If contact occurs, rinse eyes thoroughly
with water.
STOP USE AND ASK A DOCTOR IF
condition worsens or does not improve after regular use of this
product as directed
KEEP OUT OF REACH OF CHILDREN.
If swallowed, get medical help or contact a Poison Control Center
right away.
DIRECTIONS
for best results use at least twice a week or as directed by a doctor
apply to hair
massage
rinse
INACTIVE INGREDIENTS
water, cocamidopropyl betaine, disodium laureth sulfosuccinate, sodium
lauryl
sulfoacetate, decyl glucoside, sodium lauroyl sarcosinate, glycol
distearate, sodium
chloride, coco-betaine, fragrance, amodimethicone, citric acid,
PPG-5-ceteth-20, sodium
hydroxide, acrylates copolymer, sodium benzoate, carbomer, PEG-55
propylene glycol
oleate, propylene glycol, polyquaternium-39, limonene, squalane,
menthol, glycerin,
benzoic acid, trideceth-6, sodium polynaphthalenesulfonate, benzyl
salicylate, salicylic
acid, benzyl alcohol, linalool, citronellol, citral, geraniol,
cetrimonium chloride, cellulose
gum, artemisia umbelliformis flower extract, tetrasodium EDTA,
methylisothiazolinone,
potassium sorbate
KERASTASE PARIS SYMBIOSE ANTIDANDRUFF
pyrithione zinc shampoo
PRODUCT INFORMATION
PRODUCT TYPE
HUMAN OTC DRUG
ITEM CODE (SOURCE)
NDC:49967-871
ROUTE OF ADMINISTRATION
TOPICAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRENGTH
PYRITHIONE ZINC (UNII: R953O2RHZ5) (PYRITHIONE ZINC -
UNII:R953O2RHZ 5)
PYRITHIONE ZINC
10 mg in 1 mL
INACTIVE INGREDIENTS
INGREDIENT NAME
STRENGTH
WATER (UNII: 059QF0KO0R)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
DISODIUM LAURETH SULFOSUCCINATE (UNII: D6DH1DTN7E)
SODIUM LAURYL SULFOACETATE (UNII: D0Y70F2B9J)
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
SODIUM LAUROYL SARCOSINATE (UNII: 632GS996