Active Ingredient
Selenium Sulfide 1%
Careone
FDA Label NDC 41520-611
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by American Sales Company for the product Careone (NDC 41520-611). 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, purpose, uses, warnings, do not use, when using this product, stop using this product and ask a doctor if, 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
Uses
Controls flaking, scaling and itching associated with dandruff.
Warnings
For external use only
Do Not Use
- on scalp that is broken or inflamed
- if you are allergic to ingredients in this product
When Using This Product
avoid contact with eyes. If product gets into eyes, rinse eyes thoroughly with water.
Stop Using This Product 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
- shake well
- shampoo, then rinse thoroughly
- for best results, use at least twice a week or as directed by a doctor
Questions? Comments?
1 - 877 - 932 - 7948
Inactive Ingredients
Water (Aqua), Ammonium Lauryl Sulfate, Ammonium Laureth Sulfate, Dihydrogenated Tallow Phthalic Acid Amide, Cocamide DEA, Fragrance (Parfum), Titanium Dioxide, Dimethicone, Hydroxypropyl Methylcellulose, Citric Acid, Sodium Isostearoyl Lactylate, DMDM Hydantoin, Aloe Barbadensis Leaf Juice, Sodium Citrate, Sodium Chloride, Blue 1 (CI 42090)
Front And Back Labels
Image Of Label (C2)
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