FDA Label for Dawnmist Antiperspirant Deodorant
View Indications, Usage & Precautions
Dawnmist Antiperspirant Deodorant 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.
Do Not Use
on broken skin.
Discontinue Use If
■irritation and redness
develop ■ If condition persists for more than 72
hours consult a doctor.
Ask A Doctor Before Use
if you have kidney disease.
When Using This Product
■ Keep away from face and mouth ■ Do not spray near flames
Keep Out Of Reach Of Children
■If swallowed, get medical help and contact Poison Control Center right away ■ Use only as directed
Directions
Apply to underarms only. Hold two inches from underarm and spray. Use daily for best results
Inactive Ingredients
Water, Alcohol Denat, PEG-40 Hydrogenated Castor Oil, Fragrance
Package Label
DawnMist
Reduces Wetness and Odor
Clean Fresh Scent
Antiperspirant Deodorant Spray
2 FL. OZ. (59ml)
Manufactured for:
DUKAL CORPORATION
Ronkonkoma, NY 11779
(631) 656-3800
www.dukal.com
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