Active Ingredients
Ethyl Alcohol 75%
Rinse-free Gel Type Antibacterial Hand Sanitizer
FDA Label NDC 74743-002
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Guangzhou Joy Claire Biological Technology Co., Ltd for the product Rinse-free Gel Type Antibacterial Hand Sanitizer (NDC 74743-002). 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 ingredients, purpose, uses, warnings, directions, inactive ingredients, package label - principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Uses
For daily hand sanitizing
Warnings
Flammable.Keep away from heat and flame.
For external use,do not inhale or ingest.Keep out of reach of children.
Avoid contact with broken skin and keep out of eyes.In case of contact with
eyes,flush thoroughly with water.
Store below 43℃.Avoid lights and preserve in cool, dry and ventilated places. This product contains ethyl alcohol.Please test on a small area of skin before use,and stop use if skin irritation develops.
Shall not apply as sanitizing for metalware.
Directions
Rotate the pump until it pops up, gently press and pump the product into palm
of hands, then rub thoroughly over all surfaces of both hands.
Inactive Ingredients
ALOE BARBADENSIS LEAF EXTRACT, CAMELLIA SINENSIS LEAF OIL,
ROSMARINUS OFFICINALIS(ROSEMARY) LEAF OIL, AQUA,TEA-CARBOMER, PARFUM
* Please review the disclaimer below.
