Active Ingredient
Ethyl Alcohol 75%
Hand Sanitizer
FDA Label NDC 43116-030
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Shenzhen Shierjie Biological Engineering Co., Ltd for the product Hand Sanitizer (NDC 43116-030). 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, do not use, when using this product, stop use and ask a doctor if, 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
Uses
- hand sanitizer to help reduce bacteria that potentially can cause disease
- for use when soap and water are not available
Warnings
Flammable, keep away from fire/flame
For external use only
Do Not Use
- in the eyes
- on children less than 2 years of age
- on open skin wounds
When Using This Product
keep out of eyes, ears, and mouth. In case of contact, rinse thoroughly with water.
Stop Use And Ask A Doctor If
- irritation and redness develop
- condition persists for more than 72 hours
Keep Out Of Reach Of Children
If swallowed, get medical help or contact a Poison Control Center right away.
Directions
wet hands thoroughly with product and allow to dry without wiping
supervise children under 6 years of age when using this product
Other Information
- Other information a store between 15-30°C (59-86F)
- avoid freeing and excessive heat above 40°C (104F)
Inactive Ingredients
Aloe (Aloe barbadensis) Leaf Juice, Carbomer , Glycerin , Propylene Glycol , Tocopheryl Acetate ,Triethanolamine , Water
Package Label.Principal Display Panel
43116-030-01 (43116 030 01)
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