Active Ingredient(S)
Ethyl Alcohol 75%v/v
Alcohol Free Sanitizing
FDA Label NDC 74743-006
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 Alcohol Free Sanitizing (NDC 74743-006). 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, otc - keep out of reach of children, do not use, otc - when using, other information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Use
Hand sanitizer to help reduce bacteria that can potentially cause disease
For use when soap and water are not available
Warnings
For external use only.
Flammable, keep away from fire or flame
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(1-800-222-1222)
Do Not Use
On children less than 2 months of age
On open skin wounds
Otc - When Using
Keep out of eyes, ears, and mouth In case of contact with eyes, rinse eyes thoroughly with water.
Other Information
Store between 15-30C(59-86F) Avoid freezing and excessive heat above 40C (104F)
Otc - Stop Use
Stop use and ask a doctor if rritation or rash occurs. These may be signs of a serious condition
Directions
Place enough product on hands to cover all surfaces. Rub hands together until dry
Supervise children under 6 years of age when using this product to avoid swallowing
Inactive Ingredients
Aloe Barbadensis Leaf Extract, Aqua, Camellia Sinensis Leaf Oil, Carbomer, Rosmarinus Officinalis(Rosemary )Leaf oil, Parfum
* Please review the disclaimer below.
