SATINIQUE ANTI-DANDRUFF for dry, irritated scalp

Manufacturer
Amway Corp
Effective date
2021-10-26
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
legacy-cache
Hydrated at
2026-08-01 22:30:32

Label at a glance#

ProductSATINIQUE ANTI-DANDRUFF for dry, irritated scalp
Active ingredientPYRITHIONE ZINC
Label structure6 sections

Indications and uses

Controls symptoms of dandruff

Dosage and administration

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.

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients         Purpose

OTC - PURPOSE SECTION

Pyrithione Zinc 0.95% ... Anti Dandruff

Uses

INDICATIONS & USAGE SECTION

  • Controls symptoms of dandruff

Warnings

WARNINGS SECTION

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.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • 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

INACTIVE INGREDIENT SECTION

Water, Sodium Laureth Sulfate, Decyl Glucoside, Glycol Distearate, Disodium Laureth Sulfosuccinate, Glycereth-26, Sodium Chloride, Fragrance, Dimethicome, C12-15 Alkyl Lactate, Hydroxypropyl Methylcellulose, Guar Hydroxypropyltrimonium Chloride, Zinc Chloride, Hectorite, Hydroxyethylcellulose, Tetrasodium EDTA, Citric Acid, Propylene Glycol, Creatine, Tocopheryl Acetate, Limnanthes Alba (Meadowfoam) Seed Oil, Dipropylene Glycol, C10-40 Isoalkylamidopropylethyldimonium Ethosulfate, Phenoxyethanol, Magnesium Nitrate, Aloe Barbadensis Leaf Juice, Sodium Polynaphthalenesulfonate, Butyl Avocadate, PPG-12-Buteth-16, Triethanolamine, Sodium PCA, Sodium Lactate, Arginine, Xanthan Gum, Aspartic Acid, PCA, Alcohol, Glycine, Alanine, MethylChlororisothiazolinone, Ceramide NG, Serine, Magnesium Chloride, Ceramide NP, Valine, Beheric Acid, Chloesterol, Isolecine, Proline, Threonine, Methylisothiazolinone, Histidine, Phenylalanine, Perilla Ocymoides Leaf Extract, Sodium Benzoate, Potassium Sorbate, Limonene, Benzyl Salicylate, Hexyl Cinnamal, Linalool, Green 3, Blue 1.

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label3Label3

FDA-Initiated Inactive NDC Indexing#

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
PYRITHIONE ZINCACTIVE INGREDIENTR953O2RHZ52
PYRITHIONE ZINCACTIVE MOIETYR953O2RHZ52
.ALPHA.-TOCOPHEROL ACETATEINACTIVE INGREDIENT9E8X80D2L02
ALANINEINACTIVE INGREDIENTOF5P57N2ZX2
ALOE VERA LEAFINACTIVE INGREDIENTZY81Z83H0X2
ARGININEINACTIVE INGREDIENT94ZLA3W45F2
ASPARTIC ACIDINACTIVE INGREDIENT30KYC7MIAI2
BEHENIC ACIDINACTIVE INGREDIENTH390488X0A2
C12-15 ALKYL LACTATEINACTIVE INGREDIENTGC844VRD7E2
CERAMIDE 2INACTIVE INGREDIENTC04977SRJ52
CERAMIDE 3INACTIVE INGREDIENT4370DF050B2
CHOLESTEROLINACTIVE INGREDIENT97C5T2UQ7J2
CITRIC ACID MONOHYDRATEINACTIVE INGREDIENT2968PHW8QP2
CREATINEINACTIVE INGREDIENTMU72812GK02
DECYL GLUCOSIDEINACTIVE INGREDIENTZ17H97EA6Y2
DIMETHICONEINACTIVE INGREDIENT92RU3N3Y1O2
DISODIUM LAURETH SULFOSUCCINATEINACTIVE INGREDIENTD6DH1DTN7E2
EDETATE SODIUMINACTIVE INGREDIENTMP1J8420LU2
FD&C BLUE NO. 1INACTIVE INGREDIENTH3R47K3TBD2
FD&C GREEN NO. 3INACTIVE INGREDIENT3P3ONR6O1S2
GLYCERETH-26INACTIVE INGREDIENTNNE56F2N142
GLYCINEINACTIVE INGREDIENTTE7660XO1C2
GLYCOL DISTEARATEINACTIVE INGREDIENT13W7MDN21W2
GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (1.7 SUBSTITUENTS PER SACCHARIDE)INACTIVE INGREDIENTB16G315W7A2
HECTORITEINACTIVE INGREDIENT08X4KI73EZ2
HISTIDINEINACTIVE INGREDIENT4QD397987E2
HYPROMELLOSESINACTIVE INGREDIENT3NXW29V3WO2
ISOLEUCINEINACTIVE INGREDIENT04Y7590D772
MEADOWFOAM SEED OILINACTIVE INGREDIENT412ZHA4T4Y2
METHYLCHLOROISOTHIAZOLINONEINACTIVE INGREDIENTDEL7T5QRPN2
METHYLISOTHIAZOLINONEINACTIVE INGREDIENT229D0E1QFA2
PERILLA FRUTESCENS TOPINACTIVE INGREDIENTT4L5881Y682
PHENYLALANINEINACTIVE INGREDIENT47E5O17Y3R2
PIDOLIC ACIDINACTIVE INGREDIENTSZB83O1W422
PPG-12-BUTETH-16INACTIVE INGREDIENT58CG7042J12
PROLINEINACTIVE INGREDIENT9DLQ4CIU6V2
PROPYLENE GLYCOLINACTIVE INGREDIENT6DC9Q167V32
SERINEINACTIVE INGREDIENT452VLY94022
SODIUM CHLORIDEINACTIVE INGREDIENT451W47IQ8X2
SODIUM LACTATEINACTIVE INGREDIENTTU7HW0W0QT2
SODIUM LAURETH-3 SULFATEINACTIVE INGREDIENTBPV390UAP02
SODIUM PYRROLIDONE CARBOXYLATEINACTIVE INGREDIENT469OTG57A22
THREONINEINACTIVE INGREDIENT2ZD004190S2
TROLAMINEINACTIVE INGREDIENT9O3K93S3TK2
VALINEINACTIVE INGREDIENTHG18B9YRS72
WATERINACTIVE INGREDIENT059QF0KO0R2
ZINC CHLORIDEINACTIVE INGREDIENT86Q357L16B2

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 2 · 60 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
50390-00050390-000-00

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 2 · 59 matching rows.

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 9 · 502 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XSOLUTION / INTRAVENOUS90 mgExact identifier — unii candidate
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FD&C BLUE NO. 1FD&C BLUE NO. 1H3R47K3TBDLIQUID / TOPICALNAExact identifier — unii candidate
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FD&C BLUE NO. 1FD&C BLUE NO. 1H3R47K3TBDCONCENTRATE / BUCCALNAExact identifier — unii candidate
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SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XINJECTION / SUBMUCOSAL17 mgExact identifier — unii candidate
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SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XCAPSULE, EXTENDED RELEASE / ORAL41 mgExact identifier — unii candidate
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SODIUM LACTATESODIUM LACTATETU7HW0W0QTINJECTION, POWDER, LYOPHILIZED, FOR SOLUTION / INTRAVENOUS18.7 mgExact identifier — unii candidate
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FD&C GREEN NO. 3FD&C GREEN NO. 33P3ONR6O1SSHAMPOO / TOPICAL0.09 %w/wExact identifier — unii candidate
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PROPYLENE GLYCOLPROPYLENE GLYCOL6DC9Q167V3CREAM / VAGINAL1225 mgExact identifier — unii candidate
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CITRIC ACID MONOHYDRATECITRIC ACID MONOHYDRATE2968PHW8QPINJECTION / PERIDURALNAExact identifier — unii candidate
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PROPYLENE GLYCOLPROPYLENE GLYCOL6DC9Q167V3SOLUTION / DENTAL2 %w/wExact identifier — unii candidate
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EDETATE SODIUMEDETATE SODIUMMP1J8420LULOTION / TOPICAL0.17 %w/wExact identifier — unii candidate
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TROLAMINETROLAMINE9O3K93S3TKGEL / TRANSDERMAL6 mgExact identifier — unii candidate
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SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XSUSPENSION / OPHTHALMIC10 mgExact identifier — unii candidate
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CHOLESTEROLCHOLESTEROL97C5T2UQ7JOINTMENT / TOPICAL5 %w/wExact identifier — unii candidate
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CITRIC ACID MONOHYDRATECITRIC ACID MONOHYDRATE2968PHW8QPINJECTION / INTRACARDIAC1.05 %w/vExact identifier — unii candidate
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FD&C BLUE NO. 1FD&C BLUE NO. 1H3R47K3TBDCAPSULE, LIQUID FILLED / ORAL0.08 mgExact identifier — unii candidate
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HYPROMELLOSESHYPROMELLOSE3NXW29V3WOSHAMPOO / TOPICAL3 %w/wExact identifier — unii candidate
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CITRIC ACID MONOHYDRATECITRIC ACID MONOHYDRATE2968PHW8QPINJECTION, SOLUTION, CONCENTRATE / IRRIGATION1 mgExact identifier — unii candidate
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SERINESERINE452VLY9402INJECTION / INTRAVENOUS0.5 %w/vExact identifier — unii candidate
2 equally ranked IID candidates
PROPYLENE GLYCOLPROPYLENE GLYCOL6DC9Q167V3INJECTION / INTRAVENOUS16624 mgExact identifier — unii candidate
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PROPYLENE GLYCOLPROPYLENE GLYCOL6DC9Q167V3SWAB / TOPICAL34.6 %w/wExact identifier — unii candidate
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SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XINJECTION, SUSPENSION, LIPOSOMAL / EPIDURAL11 mgExact identifier — unii candidate
134 equally ranked IID candidates
SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XSUSPENSION / ENDOTRACHEAL7.6 mgExact identifier — unii candidate
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HYPROMELLOSESHYPROMELLOSE3NXW29V3WOCAPSULE, COATED, EXTENDED RELEASE / ORALNAExact identifier — unii candidate
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SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XLOTION / TOPICAL0.3 %w/vExact identifier — unii candidate
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SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XSHAMPOO / TOPICAL150 mgExact identifier — unii candidate
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CITRIC ACID MONOHYDRATECITRIC ACID MONOHYDRATE2968PHW8QPLIQUID / ORAL114 mgExact identifier — unii candidate
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TROLAMINETROLAMINE9O3K93S3TKLOTION / TOPICAL360 mgExact identifier — unii candidate
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GLYCINEGLYCINETE7660XO1CINJECTION, POWDER, LYOPHILIZED, FOR SOLUTION / INTRAVENOUS200 mgExact identifier — unii candidate
20 equally ranked IID candidates
CITRIC ACID MONOHYDRATECITRIC ACID MONOHYDRATE2968PHW8QPINJECTION, SOLUTION, CONCENTRATE / INTRAOCULAR1 mgExact identifier — unii candidate
88 equally ranked IID candidates
CITRIC ACID MONOHYDRATECITRIC ACID MONOHYDRATE2968PHW8QPSOLUTION / INTRAOCULAR1 mgExact identifier — unii candidate
88 equally ranked IID candidates
CITRIC ACID MONOHYDRATECITRIC ACID MONOHYDRATE2968PHW8QPSPRAY / NASAL9 mgExact identifier — unii candidate
88 equally ranked IID candidates
FD&C GREEN NO. 3FD&C GREEN NO. 33P3ONR6O1SSOLUTION / ORAL0.25 mg/5mlExact identifier — unii candidate
15 equally ranked IID candidates
CITRIC ACID MONOHYDRATECITRIC ACID MONOHYDRATE2968PHW8QPINJECTION / SUBCUTANEOUS28 mgExact identifier — unii candidate
88 equally ranked IID candidates
SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XSPRAY / NASAL30 mgExact identifier — unii candidate
134 equally ranked IID candidates
CHOLESTEROLCHOLESTEROL97C5T2UQ7JCREAM / TOPICAL1 %w/wExact identifier — unii candidate
10 equally ranked IID candidates
PROPYLENE GLYCOLPROPYLENE GLYCOL6DC9Q167V3DROPS / ORAL200 mg/1mlExact identifier — unii candidate
81 equally ranked IID candidates
ARGININEARGININE94ZLA3W45FINJECTION / INTRAVENOUS790 mgExact identifier — unii candidate
11 equally ranked IID candidates
GLYCINEGLYCINETE7660XO1CPASTE, DENTIFRICE / DENTAL0.34 %w/wExact identifier — unii candidate
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SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XINJECTION / INTRATUMOR1.2 %w/vExact identifier — unii candidate
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TROLAMINETROLAMINE9O3K93S3TKSOAP / TOPICAL0.08 %w/wExact identifier — unii candidate
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SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XPOWDER, FOR SUSPENSION / ENDOTRACHEAL46.76 mgExact identifier — unii candidate
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CITRIC ACID MONOHYDRATECITRIC ACID MONOHYDRATE2968PHW8QPTABLET, ORALLY DISINTEGRATING, DELAYED RELEASE / ORAL2 mgExact identifier — unii candidate
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CITRIC ACID MONOHYDRATECITRIC ACID MONOHYDRATE2968PHW8QPINJECTION / INTRATHECALADJ PHExact identifier — unii candidate
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SODIUM LACTATESODIUM LACTATETU7HW0W0QTSOLUTION / TOPICAL0.93 %w/wExact identifier — unii candidate
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SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XINJECTION, SOLUTION / INTRAMUSCULAR1486 mgExact identifier — unii candidate
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GLYCINEGLYCINETE7660XO1CINJECTION / INTRAMUSCULAR68 mgExact identifier — unii candidate
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SODIUM LAURETH-3 SULFATESODIUM LAURETH-3 SULFATEBPV390UAP0CAPSULE / ORAL3.5 mgExact identifier — unii candidate
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CITRIC ACID MONOHYDRATECITRIC ACID MONOHYDRATE2968PHW8QPTABLET, ORALLY DISINTEGRATING / ORAL83 mgExact identifier — unii candidate
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openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
eac43df5-0662-08c3-e053-2995a90a2564c73ef471-8904-436f-9e98-d0d74dc25f602022-10-11WarningsExact identifier
spl set id: c73ef471-8904-436f-9e98-d0d74dc25f60

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.