Active Ingredient
Ethyl Alcohol 70% v/v.
Hand Sanitizer
FDA Label NDC 77106-002
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Resource Recovery & Trading Llc for the product Hand Sanitizer (NDC 77106-002). 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, otc - keep out of reach of children, directions, inactive ingredients, product label, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Uses
As an external disinfectant. Suitable for application on hand. Rub the gel upon application. Recommended for repeated use. Suitable fo use above ago 2 year.
Warnings
For external use only.
Flammable - Keep away from heat or flame.
When using this product avoid contact with the eyes. If contact occurs, rinse eyes thoroughly with water.
Stop using and ask doctor if irritation or redness develop and last more than 72 hours.
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
Apply a small amount in your palm and rub hands together briskly until dry.
Children under 6 should be supervised when using this product.
Other information
Do not store above 105°F (40°C).
May discolor certain wood surfaces.
Questions ?
Call +1 954-773-0003
Inactive Ingredients
Purified water, carbomer, triethanolamine, glycerin, propylene glycol, fragrance, Aloe Barbadensis leaf juice.
Product Label
Label (Label)
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