Dawnmist Antiperspirant And Deodorant
FDA Label NDC 55504-0230

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Donovan Industries, Inc. for the product Dawnmist Antiperspirant And Deodorant (NDC 55504-0230). 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, uses, warnings, when using this product, keep out of reach of children., directions, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

Aluminum Chlorohydrate 7.90%

Purpose

Antiperspirant

Uses

Reduces underarm perspiration

Warnings

For external use only

Do not use on broken skin.

Stop use if rash or irritation occurs

Ask a doctor before use if you have kidney disease

When Using This Product

  • Keep away from face and mouth to avoid breathing it
  • do not spray near flames

Keep Out Of Reach Of Children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Apply to underarms only.

Inactive Ingredients

Water, SD Alcohol 40-B, Glycerin, PEG-40 Hydrogenated Castor Oil, Diazolidinyl Urea, Fragrance, Iodopropynyl Butylcarbamate

Manufactured For:


DONOVAN INDUSTRIES, INC.
TAMPA, FL 33626-3061
800.334.4401
WWW.DAWNMIST.COM

MADE IN CHINA

Package Label.Principal Display Panel

DawnMist

Reduces Wetness and Odor

Clean Fresh Scent

Antiperspirant

Deodorant

Spray


Product Container Label

Dawnmist Antiperspirant Deodorant (Dawnmistdeodorant)

Dawnmist Antiperspirant Deodorant (Dawnmistdeodorant)

* Please review the disclaimer below.