Otc - Active Ingredient
Active Ingredient:
Benzethonium Chloride: 0.1%
Deodorant
FDA Label NDC 73027-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Jiangsu Hanhe Daily Chemicals Co., Ltd. for the product Deodorant (NDC 73027-001). 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 - ask doctor, otc - keep out of reach of children, dosage & administration, inactive ingredient, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Purpose:
Antibacterial
Indications & Usage
Uses:
For washing to decrease bacteria on skin
Warnings
Warnings:
External use only
When using this product, avoid contact with eyes. In case of eye contact, fush with water.
If swallowed, get medical help or contact a Poison Control Center right away.
Otc - Ask Doctor
Stop use and ask doctor if irritation and redness develop
Otc - Keep Out Of Reach Of Children
Do not use this product on infants under age of 6
Keep out of reach of children.
Dosage & Administration
Wet bar with water
Lather vigorously and wash skin
Rinse and dry thoroughly
Inactive Ingredient
Inactive Ingredients:
Soap (Sodium Palmate, and/or Sodium Tallowate, Sodium Cocoate, and/or Sodium Palm Kernelate), Calcium Carbonate, Water, Glycerin, Sodium Chloride, Sodium Hydroxide, Fragrance, Tetrasodium EDTA, Etidronate Tetrasodium
Package Label.Principal Display Panel
Image Description (Label)
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