FDA Label for Dawnmist Antiperspirant
View Indications, Usage & Precautions
Dawnmist Antiperspirant Product Label
The following document was submitted to the FDA by the labeler of this product Dukal Llc. 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.
Active Ingredient
Aluminum Chlorohydrate 4.5%
Purpose
Antiperspirant
Use
Reduces underarm perspiration
Warnings
For external use only.
Flammable, keep away from fire or flame.
Do Not Use
Do not use on broken skin
Stop Use
Stop use if rash or irritation occurs.
Ask A Doctor Before Use
Ask a doctor before use if you have kidney disease.
Keep Out Of Reach Of Children
Keep out of reach of children. If accidently swallowed, get medical help or contact Poison Control Center right away.
Directions
Apply to underarms only.
Inactive Ingredients
Alcohol, Fragrance, PEG-40 Hydrogenated Castor Oil, Water
Package Label.Principal Display Panel
NDC 65517-2030-1
DawnMist
Personal Care
Antiperspirant
Spray
Fresh Scent
2FL.OZ. (59ml)
Principle Display Panel
NDC 65517-2030-2
DawnMist
Personal Care
Antiperspirant
Spray
Fresh Scent
4FL.OZ. (118ml)
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