Otc - Active Ingredient
Aluminum Chloride- 12%
Zerosweat Antiperspirant 12%
FDA Label NDC 65112-306
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by I. Shay Cosmetics for the product Zerosweat Antiperspirant 12% (NDC 65112-306). 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 otc - active ingredient, otc - purpose, otc - keep out of reach of children, indications & usage, inactive ingredient, warnings, dosage & administration, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Antiperspirant
Otc - Keep Out Of Reach Of Children
WARNING: Keep out of reach of children
Indications & Usage
Decreases excessive perspiration.
Decreases underarm sweating.
Inactive Ingredient
Purified Water, Aloe Vera Extract, Allantoin, Willow Bark Extract, Chamomile Extract, Glycerin, Sodium Bicarbonate.
Warnings
For External Use Only.
Ask a doctor before use if you have kidney disease.
Do not use:
-Immediately after shaving
-On irritated skin
-On broken skin
-Immediately after bathing
When using this product do not use in or near eyes.
Stop use and ask doctor if rash or irritation develops
Keep out of reach of children.
If swallowed, get medical help or contact a Poison Control Center right away.
Dosage & Administration
Apply to appropriate body area. Apply sparingly. Apply only a few strokes under each arm. Apply only at bedtime.
* Please review the disclaimer below.
