Active Ingredient(S)
Selenium Sulfide 1%
Uchoize S2 Balance Anti-dandruff Shampoo
FDA Label NDC 85724-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Dreamwise International Corp for the product Uchoize S2 Balance Anti-dandruff (NDC 85724-001). 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 ingredient(s), purpose, use, warnings, do not use, otc - when using, otc - stop use, otc - keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Anti-dandruff
Use
Controls the symptoms of:
dandruff, seborheic dermatitis, psoriasis.
Warnings
For external use only
Do Not Use
If pregnant or breast-feeding, ask a doctor before use.
Otc - When Using
avoid contact with the eyes. If contact occurs,rinse eyes
thoroughly with water,
Otc - Stop Use
rash appears
condition worsens or does not improve in 2-4 weeks
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or
contact a Poison Control Center (1-800-222-1222) right away,
Directions
adults and children 12 years and over
1. wet hair thoroughly
2. apply shampoo, generously lather, rinse thoroughly. Repeat
3. use every 3-4 days for up to 8 weeks or as directed by a doctor, Then use only as needed to control dandruff
children under 12 years
1. ask a doctor
Other Information
store at 20°C to 25°C (68°F-77°F)
see bottom panel for expiration date
Inactive Ingredients
Aqua,DecyI Glucoside, Sodium C14-16 Olefin Sulfonate, Cocamidopropyl Betaine, Glycerol, Glycol Stearate, Sodium
Benzoate, Phenoxyethanol, Thuja Orientalis Leaf Extract, Ginger Root Extract, Panthenol, Menthol, Polyquaternium-10,
Zinc Pca, Sodium Hyaluronate, Citric Acid
Package Label - Principal Display Panel
Undefined (Label)
* Please review the disclaimer below.
