Sanitize Asap Hand Sanitizer
FDA Label NDC 73871-377
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 73871-377). 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, otc - active ingredient, otc - purpose, indications & usage, warnings, 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 - Active Ingredient
Active ingredient:
Isopropyl Alcohol 70%
Otc - Purpose
Purpose
Antiseptic
Indications & Usage
Uses: to decrease bacteria on the skin that could interfere with good health, recommended for repeated use.
Warnings
Warnings
Flammable, keep away from heat and flame.
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.
Dosage & Administration
Directions: wet the hands thoroughly with the product and allow to dry without wiping.
Inactive Ingredient
Inactive Ingredients:
Alcohol, Deionized water, Hydroxypropyl guar, Eucalyptus globulus
Other
ANTI-BACTERIAL
KILLS 99.99% OF GERMS
MADE IN USA
LABORATORY CRAFTED - ANTI-BACTERIAL BLEND FROM THE RESEARCH LABORATORIES OF NWH.
BE SAFE BE CAUTIOUS
SANITIZEASAP.COM
New World Cosmetics and Medicinals.
1080 Holland Drive. Suite 1
Boca Raton, Florida 33487
These statements have not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat cure or prevent any disease.
Packaging
Asap1 (Besafe 1)
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