The following Structured Product Label (SPL) was submitted to the FDA by Conopco Inc. D/b/a Unilever for the product Axe (NDC 64942-1185). 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, indications & usage, warnings, otc - when using, otc - stop use, otc - keep out of reach of children, dosage & administration, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Otc - Active Ingredient
Active Ingredient
Pyrithione Zinc (1.0%)
Otc - Purpose
PurposeAnti-dandruff
Indications & Usage
Usecontrols scalp itching and flaking associated with dandruff
Warnings
WarningsFor external use only
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.
Dosage & Administration
Directions· Squeeze. Lather. Rinse· For best results, use at least twice a week or as directed by a doctor.
Inactive Ingredient
Inactive ingredientsWater (Aqua), Sodium Laureth Sulfate, Cocamidopropyl Betaine, Sodium
Chloride, Fragrance (Parfum), Carbomer, Dimethiconol, Glycol
Distearate, Menthol, DMDM Hydantoin, Guar Hydroxypropyltrimonium
Chloride, TEA-Dodecylbenzenesulfonate, Citric Acid, Iodopropynyl
Butylcarbamate, Methylchloroisothiazolinone, Methylisothiazolinone,
PPG-9, Mica (CI 77019), Titanium Dioxide (CI 77891), Blue 1 (CI
42090), Red 33 (CI 17200)
Otc - Questions
theaxeeffect.com
QUESTIONS/COMMENTS?
1-800-450-7580
Package Label.Principal Display Panel
PDP 12 oz front
PDP 12 oz back
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