Active Ingredient(S)
Ethyl Alcohol 70% v/v. Purpose: Antimicrobial
Hand Sanitizer
FDA Label NDC 76846-1011
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Xiamen Luwei Industrial Co., Ltd for the product Hand Sanitizer (NDC 76846-1011). 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(s), purpose, use, warnings, do not use, otc - when using, otc - stop use, otc - 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
Purpose
Antiseptic hand rub.
Use
Kills 99.9% of most common germs.
Use in the absence of water or towels.
Warnings
For external use only.
Flammable, keep away from fire or flame.
Do not mix with detergent or other chemicals.
Do Not Use
Avoid contact with eyes or wound, if product gets into eyes, rinse thoroughly with water.
Otc - When Using
When using this product, do not use in or near the eyes or wound.
Use in well ventilated environment.
Otc - Stop Use
Stop using this product if skin irritation occurs and consult a doctor immediately.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children.
If swallowed, seek medical help immediately.
Directions
- Dispense product evenly on palms or on material surface and rub your hands until dry.
- Children should be under adult supervision when using this product.
- No dilute required.
Other Information
- Store at room temperature.
- Product may cause discoloration on certain fabrics or materials.
Inactive Ingredients
Water, Carbomer, Triethanolamine, Aloe extract, Essence.
Package Label - Principal Display Panel
050-1 (050 1)
050-2 (050 2)
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