Active Ingredient
Ethyl Alcohol 70% v/v. Purpose: Antiseptic
Hand Sanitizer Premium Formula
FDA Label NDC 73812-002
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Ltp Global for the product Hand Sanitizer Premium Formula (NDC 73812-002). 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, use, warnings, otc - when using, otc - stop use, otc - 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
Use
- to decrease bacteria on the skin that could cause disease
Warnings
For external use only : hands
Flammable. Keep away from heat or flame.
Otc - When Using
When using this product
- keep out of eyes. In case of contact with eyes, flush thoroughly with water.
- avoid contact with broken skin
- do not inhale or ingest
Otc - Stop Use
Stop use and ask a doctor if
- irritation or rash occurs. These may be signs of serious condition.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Directions
- Put enough product in your palm to cover hands and rub hands together briskly until dry
- Children under 6 years should be supervised when using this product
Other Information
- Store between 59-86°F (15-30°C)
- Avoid freezing and excessive heat above 104°F (40°C)
- Do not use on children under two months of age.
Inactive Ingredients
Water, Glycerin, Carbomer, Trolamine, L-Menthol, Green Tea Leaf, Aloe Vera Leaf
Package Label - Principal Display Panel
Pouch Label (73812 002 02)
Out Box Label (73812 002 05)
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