Active Ingredients
Ethyl Alcohol 70%v/v.
Purpose: Antiseptic
Sanihealth Labs Hand Sanitizer
FDA Label NDC 79861-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Sanihealth Labs Inc. for the product Sanihealth Labs Hand Sanitizer (NDC 79861-001). 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 active ingredients, purpose, safety instructions, ask doctor, keep out of reach of children, other information, inactive ingredients, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Safety Instructions
Flammable, Keep away from fire and flame
Ask Doctor
Stop Use and Ask a doctor if irritation or redness develops
Keep Out Of Reach Of Children
If swallowed, get medical help or contact Poison Control right away
Other Information
Store below 15-30°C
May discolor certain fabrics or surfaces.
Avoid freezing and excessive heat
Inactive Ingredients
water, hydrolyzed jojoba esters, glycerin, fragrance, denatonium benozate
Directions
- Place enough product in your palm to thoroughly cover your hands
- Rub hands together briskly until dry
- Children should be supervised when using this product.
- For personal and occasional domestic use
Warnings
For external use only.
Flammable. Keep away from fire or flame.
Uses
- helps reduce bacteria on the skin that could cause disease
Package Label.Principal Display Panel
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