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 7.8%
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.
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.
Inactive Ingredients
Water, Hydroxyethyl Cellulose, Propylene Glycol, Diazolidinyl Urea, Iodopropynyl Butylcarbamate, Polysorbate 20, Menthol
Principal Display Panel - Bottle Label
DawnMist®
DEODORANTS
Roll-On
Antiperspirant
REDUCES WETNESS & ODOR
FRESH SCENT
1.5 FL. OZ. (44ml)
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