Active Ingredient
Ethyl Alcohol 75 % v/v.
999 Hand Sanitizer
FDA Label NDC 76536-391
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Ler V Trading Inc. for the product 999 Hand Sanitizer (NDC 76536-391). 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, other information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Uses
Hand sanitizer to help reduce bacteria on the skin.
Warnings
Flammable. Keep away from fire or flame.
For external use only.
When using this product, do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation or rash appears and lasts.
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.
Inactive Ingredients
Water(Aqua), Glycerin, Carbomer Homopolymer, Trolamine, Fragrance (Parfum).
Other Information
STORE BETWEEN 59-86℉(15-30℃)
AVOID FREEZING AND EXCESSIVE HEAT ABOVE 140℉(40℃)
EXP DATE: SEE ON PACKAGE
Product Labels
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