Sanitize Asap Hand Sanitizer
FDA Label NDC 73871-378
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by New World Holdings, Inc. for the product Sanitize Asap Hand Sanitizer (NDC 73871-378). 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 drug facts, active ingredient:, purpose:, inactive ingredients:, warnings, otc - keep out of reach of children, packaging, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient:
Ethyl Alcohol Denatured.................80%
Purpose:
Antiseptic
Inactive Ingredients:
Deionized Water, Hydroxypropyl Cellulose, Glycerin, Hydrogen Peroxide.
Warnings
Otc - Keep Out Of Reach Of Children
Keep out of reach of children, keep out of the eyes, avoid contact with broken skin, if swallowed get medical help or contact a poison control center.
Flammable, keep away from heat and flame.
Packaging
Image (Label1)
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