First Hand Hand Sanitizer
FDA Label NDC 78705-000
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by South Tenth Development, Llc for the product First Hand Hand Sanitizer (NDC 78705-000). 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, uses, warnings, when using this product, stop use & ask a doctor, keep out of reach of children., and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient
Ethyl Alcohol 80%
Purpose
Antiseptic
Uses
Reduce bacteria on the skin. Recommended for repeated use
Warnings
For external use only.
Flammable Keep away from fire, flame, or sparks
When Using This Product
do not use in or near eyes. In case of contact, rinse eyes thoroughly with water
Stop Use & Ask A Doctor
If irritation or rash appears on the skin.
Keep Out Of Reach Of Children.
If swallowed, get medical help or contact a Poison Control Center right away.
Directions
- Place enough to cover both hands in the palm, and rub hands together until dry.
- Children under 6 years of age should be supervised by an adult when applying this product.
Other Information
- Store below 105°F.
- May discolor certain fabrics or surfaces.
Inactive Ingredients
Distilled water, glycerol, hydrogen peroxide, denatonium benzoate.
Package Labeling
Label (Label)
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