Active Ingredient
Aluminum Chlorohydrate 4.5%
Dawnmist Antiperspirant Deodorant Liquid
FDA Label NDC 65517-1008
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Dukal Llc for the product Dawnmist Antiperspirant Deodorant (NDC 65517-1008). 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 active ingredient, purpose, use, warnings, do not use, discontinue use if, ask a doctor before use, when using this product, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
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
Label (Label)
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