FDA Label for Axe Freeze Antidandruff
View Indications, Usage & Precautions
Axe Freeze Antidandruff Product Label
The following document was submitted to the FDA by the labeler of this product Conopco Inc. D/b/a Unilever. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.
Otc - Active Ingredient
Active Ingredient
Pyrithione Zinc (1.0%)
Otc - Purpose
Purpose
Anti-dandruff
Indications & Usage
Use helps control scalp itching and flaking associated with dandruff.
Warnings
Warnings
For external use only
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.
Otc - Stop Use
Avoid contact with eyes. Product contains menthol. If you experience discomfort, please stop use.
Stop use and ask a doctor if condition worsens or does not improve after regular use of this product as directed.
Dosage & Administration
Direction
· Squeeze. Lather. Rinse
· For best results, use at least twice a week or as directed by a doctor.
Inactive Ingredient
Inactive ingredients
Water (Aqua), Sodium Laureth Sulfate, Cocamidopropyl Betaine, Sodium Chloride, Fragrance (Parfum), Carbomer, Dimethiconol, Menthol, DMDM Hydantoin, Citric Acid, Guar Hydroxypropyltrimonium Chloride, TEA-Dodecylbenzenesulfonate, Butylene Glycol, Iodopropynyl Butylcarbamate, Propylene Glycol, PPG-9, Methylisothiazolinone, Methylchloroisothiazolinone, Blue 1 (CI 42090), Yellow 5 (CI 19140).
Otc - Questions
theaxeeffect.com
QUESTIONS/COMMENTS?
1-800-450-7580
12 Fl Oz Pdp
12 Fl Oz Back
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