Zerosweat
FDA Label NDC 55726-048

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Zerosweat Inc for the product Zerosweat (NDC 55726-048). 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, indications & usage, warnings, otc - do not use, otc - when using, otc - stop use, otc - ask doctor, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Otc - Active Ingredient

Active Ingredients: Aluminum Chloride 15%

Otc - Purpose

Purpose: Antiperspirant

Indications & Usage

Uses

  • Treats Excessive Perspiration
  • Reduces underarm wetness

Warnings

Warnings:

For external use only.

Otc - Do Not Use

Do not use:

  • Immediately after shaving
  • On broken skin
  • On irritated skin
  • Immediately after bathing

Otc - When Using

When using this product

  • Do not use in or near eyes
  • Apply to underarms only.

Otc - Stop Use

Stop use and ask a doctor if rash or irritation develops.

Otc - Ask Doctor

Ask a doctor before use if you have kidney disease.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children.

If swallowed, get medical help or contact a poison control center right away.

Dosage & Administration

Directions

  • Apply to underarms only.
  • Apply only at bedtime.
  • Apply sparingly.
  • Apply only a few strokes under each arm,

Inactive Ingredient

Inactive Ingredients: Sodium bicarbonate,water

Principal Display Panel - 35.5 Ml Bottle Carton

Z
ZERO SWEAT

Antiperspirant

Up To 7 Day Protection

Keeps You Dry.
Guaranteed.

1.2 FL. OZ (35.5 ml.)

Principal Display Panel (35.5 ml Bottle Carton)

Principal Display Panel (35.5 ml Bottle Carton)

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