Otc - Active Ingredient
Active Ingredient Purpose
Pyrithione Zinc (1.0%)....Anti-dandruff
Axe
FDA Label NDC 64942-1049
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Conopco Inc. D/b/a Unilever for the product Axe (NDC 64942-1049). 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 otc - active ingredient, otc - purpose, warnings, otc - when using, otc - stop use, otc - keep out of reach of children, inactive ingredient, otc - questions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Use controls scalp itching and flaking associated with dandruff.
Warnings
For external use only (see inside of label)
Otc - When Using
When using this product avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.
Otc - Stop Use
Stop use and ask a doctor if condition worsens or does not improve after regular use of this product as directed.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Inactive Ingredient
Water (Aqua), Sodium Laureth Sulfate, Cocamidopropyl Betaine, Sodium Chloride, Fragrance (Parfum), Carbomer, Dimethiconol, Glycol Distearate, DMDM Hydantoin, Guar Hydroxypropyltrimonium Chloride, TEA-Dodecylbenzenesulfonate, Iodopropynyl Butylcarbamate, Methylchloroisothiazolinone, Methylisothiazolinone, PPG-9, Citric Acid, Mica (CI 77019), Titanium Dioxide (CI 77891), Blue 1 (CI 42090), Yellow 5 (CI 19140).
Otc - Questions
Questions/Comments?
1-800-450-7580
theaxeeffect.com
Package Label.Principal Display Panel
PDP 12 oz front
PDP 12 oz back
PDP 12 oz back
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