Active Ingredient
Isopropyl alcohol 70%, USP
Benemax Advanced Hand Sanitizer
FDA Label NDC 73700-002
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Nugale Pharmaceutical Inc for the product Benemax Advanced Hand Sanitizer (NDC 73700-002). 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 active ingredient, purpose, uses, warnings, when using this product, stop use and ask a doctor, keep out of reach of children., directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Uses
as a hand sanitizer when there is no water, to reduce bacteria on the skin which can cause illness. Recommended for repeated use.
Warnings
Flammable, keep away from fire or flame
For external use only
When Using This Product
- do not use in or near the eyes, or inhale
- in case of contact, rinse eyes thoroughly with water
Stop Use And Ask A Doctor
if a rash on irritation appear and remain at the site of contact
Keep Out Of Reach Of Children.
If swallowed, get medical help right away or contact a Poison Control Center immediately.
Directions
- dispense sufficient liquid to cover the hands, rub hands together briskly for 30 seconds.
Allow hands to dry.
• children under 6 years of age must be upervised when using this product.
Other Information
- do not store above 1100F (430C). May discolor certain fabrics or substances
Inactive Ingredient
Aloe (aloe barbadensis) Juice, D-alpha-tocopheryl Acetate, Glycerin, PEG, Water
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