SATINIQUE ANTI DANDRUFF- pyrithione zinc cream

Satinique Anti Dandruff by

Drug Labeling and Warnings

Satinique Anti Dandruff by is a Otc medication manufactured, distributed, or labeled by Access Business Group LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredients

Pyrithione Zinc 0.95%

Purpose

Anti Dandruff

Uses

• Controls symptoms of dandruff

Warnings

For external use only.

Avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.

If condition worsens or does not improve after regular use, consult a doctor.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• Shake well before use.
• Wet hair. Apply shampoo and work into a lather. Rinse thoroughly.
• For best result, use at least twice a week or as directed by a doctor.

Inactive Ingredients

Water, Sodium Laureth Sulfate, Decyl Glucoside, Glycol Distearate, Disodium Laureth Sulfosuccinate, Glycereth-26, Ceramide 2 , Ceramide-3, C10-40 isoalkylamidopropylethyldimonium ethosulfate, Creatine, Fragrance, Dimethicome, Sodium Chloride, C12-15 Alkyl Lactate, Hydroxypropyl Methylcellulose, Guar Hydroxypropyltrimonium Chloride, Zinc Chloride, Hectorite, Hydroxyethylcellulose, Tetrasodium EDTA, Citric Acid, Tocopheryl Acetate, Limnanthes Alba (Meadowfoam) Seed Oil, Propylene Glycol, Aloe Barbadensis Leaf Juice, Butyl Avodate, PPG-12-Buteth-15, Triethanolamine, Sodium PCA, Sodium Lactate, Arginine, Aspartic Acid, PCA, Glycine, Alanine, MethylChlororisothiazolinone, Serine, Valine, Behenic Acid, Cholesterol, Isoleucine, Proline, Threonine, Methylisothiazolinone, Histidine, Phenylalanine, Perilla Ocymoides Leaf Extract, Green 3, Blue 1.

Package Labeling:

INGREDIENTS AND APPEARANCE

SATINIQUE ANTI DANDRUFF 
pyrithione zinc cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 10056-006
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PYRITHIONE ZINC (UNII: R953O2RHZ5) (PYRITHIONE ZINC - UNII:R953O2RHZ5)	PYRITHIONE ZINC	95 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
SODIUM LAURETH-3 SULFATE (UNII: BPV390UAP0)
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
GLYCOL DISTEARATE (UNII: 13W7MDN21W)
DISODIUM LAURETH SULFOSUCCINATE (UNII: D6DH1DTN7E)
GLYCERETH-26 (UNII: NNE56F2N14)
CERAMIDE 2 (UNII: C04977SRJ5)
CERAMIDE 3 (UNII: 4370DF050B)
CREATINE (UNII: MU72812GK0)
DIMETHICONE (UNII: 92RU3N3Y1O)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
C12-15 ALKYL LACTATE (UNII: GC844VRD7E)
HYPROMELLOSES (UNII: 3NXW29V3WO)
GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (1.7 SUBSTITUENTS PER SACCHARIDE) (UNII: B16G315W7A)
ZINC CHLORIDE (UNII: 86Q357L16B)
HECTORITE (UNII: 08X4KI73EZ)
EDETATE SODIUM (UNII: MP1J8420LU)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
MEADOWFOAM SEED OIL (UNII: 412ZHA4T4Y)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
PPG-12-BUTETH-16 (UNII: 58CG7042J1)
TROLAMINE (UNII: 9O3K93S3TK)
SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
SODIUM LACTATE (UNII: TU7HW0W0QT)
ARGININE (UNII: 94ZLA3W45F)
ASPARTIC ACID (UNII: 30KYC7MIAI)
PIDOLIC ACID (UNII: SZB83O1W42)
GLYCINE (UNII: TE7660XO1C)
ALANINE (UNII: OF5P57N2ZX)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
SERINE (UNII: 452VLY9402)
VALINE (UNII: HG18B9YRS7)
BEHENIC ACID (UNII: H390488X0A)
CHOLESTEROL (UNII: 97C5T2UQ7J)
ISOLEUCINE (UNII: 04Y7590D77)
PROLINE (UNII: 9DLQ4CIU6V)
THREONINE (UNII: 2ZD004190S)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
HISTIDINE (UNII: 4QD397987E)
PHENYLALANINE (UNII: 47E5O17Y3R)
PERILLA FRUTESCENS LEAF (UNII: T4L5881Y68)
FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 10056-006-01	280 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/29/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part358H	03/29/2017

Labeler - Access Business Group LLC (839830713)