Active Ingredient
Aluminum Chlorohydrate 7.8%
Dawnmist Antiperspirant Lotion
FDA Label NDC 65517-2033
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 (NDC 65517-2033). 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, ask a doctor before use, keep out of reach of children, directions, 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
Do not use on broken skin
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
Diazolidinyl Urea, Disodium EDTA, Fragrance, Glycerin, Hydroxypropyl Methyl Cellulose, Methylparaben, PEG-40 Hydrogenated Castor Oil, Triethylamine, Water
Package Label.Principal Display Panel
NDC 65517-2033-1
DawnMist
Personal Care
Clear Roll-On
Antiperspirant
Fresh Scent
1.5FL.OZ. (44ml)
Rd7990 (Rd7990)
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