Sanitize Asap Hand Sanitizer
FDA Label NDC 73871-379
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 73871-379). 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, 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, Glycerin, Hydrogen peroxide.
Warnings
Packaging
Image (Label1)
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