Dawnmist Antiperspirant Deodorant Lotion
FDA Label NDC 65517-1021

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 65517-1021). 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, keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

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)

Principal Display Panel (Bottle Label)

Principal Display Panel (Bottle Label)

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