Active Ingredients
Pyrithione Zinc 0.95%
The following Structured Product Label (SPL) was submitted to the FDA by Access Business Group Llc for the product Satinique Anti Dandruff (NDC 10056-006). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredients, purpose, uses, warnings, keep out of reach of children., directions, inactive ingredients, package labeling:, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Pyrithione Zinc 0.95%
Anti Dandruff
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.
If swallowed, get medical help or contact a Poison Control Center right away.
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.
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