Active Ingredient
Aluminum Chlorohydrate 20.2%
Dry Orignal Fresh 3.5oz
FDA Label NDC 57337-152
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Rejoice International Corp. for the product Dry Orignal Fresh 3.5oz (NDC 57337-152). 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, do not use, otc - when using, ask a doctor, 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
Purpose
Antiperspirant
Uses
Reduces underarm wetness
Warnings
Flammable. Do not use near heat, flame or while smoking. Can cause serious injury or death
Do Not Use
Do not use on broken or irritated skin. Stop use if rash or irritation develops.
Otc - When Using
- Keep away from face and mouth to avoid breathing in
- Avoid spraying in eyes. Contents under pressure. Do not puncture or incinerate. Do not expose to heat or store at temperatures above 120°F/50°C or enclosed places that could overheat.
- USE ONLY AS DIRECTED. INTENTIONAL MISUSE BY DELIBERATELY CONCENTRATING AND INHALING THE CONTENT CAN BE HARMFUL OR FATAL.
Ask A Doctor
Ask a doctor before using, if you have kidney disease.
Keep Out Of Reach Of Children
Keep out of reach of children
Directions
For undearm use only. Shake can well before each use. Hold can 6 inches away from skin. Spray underarm.
Inactive Ingredients
Cyclopentasiloxane
Butane
Propane
Isobutane
Hydrofluorocarbon 152A
PPG-14 Butyl Ether
C12-15 Alkyl Benzoate
Helianthus Annuus (Sunflower) Seed Oil
Fragrance
BHT
Dimethiconol
Disteardimonium Hectorite
Octldodecanol
Propylene Carbonate
Tocopheryl Acetate
Package Label.Principal Display Panel
Label (Label)
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