Active Ingredient(S)
Ethyl Alcohol 67% w/w. Purpose: Antimicrobial
Hand Sanitizer
FDA Label NDC 77309-101
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Ningbo Roni Cosmetic Co., Ltd for the product Hand Sanitizer (NDC 77309-101). 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
Antimicrobial.
Use
Uses for handwashing to decrease bacteria on the skin.
Warnings
For external use only.
Flammable, keep away from heat and flame.
Do Not Use
Do not us in the eyes. In case of contact, rinse eyes troroughly with water.
Otc - When Using
When using this product, do not use in or near the eyes or wound.
Otc - Stop Use
Stop use and ask a doctor if irritation and redness develop and persist for 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
- 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 20℃ to 25℃.
Inactive Ingredients
Aqua, Carbomer, Triethanolamine, Aloe barbadensis leaf juice, Tocopherol, Fragrance.
Package Label - Principal Display Panel
59 (59)
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