Active Ingredient(S)
Ethyl Alcohol 70% v/v. Purpose: Antiseptic
Ibrite Hand Sanitizer
FDA Label NDC 10129-080
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Gingi-pak for the product Ibrite Hand Sanitizer (NDC 10129-080). 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, 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
Use
Reduce bacteria that potentially can cause disease.
Recommened for repeated use
Warnings
For external use only. Flammable. Keep away from heat or flame
Do Not Use
Do not apply around eyes.
When Using This Product
- keep out of eyes. In case of contact with eyes, flush thoroughly with water.
- Avoid contact with broken skin.
- Do not inhale or ingest.
Stop Use And Ask A Doctor If
irritation or rash occurs. These may be signs of a serious condition.
Keep Out Of Reach Of Children.
If swallowed, get medical help or contact a Poison Control Center right away.
Directions
- Dispense enough gel in your palm to cover all surfaces of hands and finger. Rub hands together vigorously until dry.
- Usage on children requires adult supervision, not recommended for infants.
- Work best on clean and dry hands.
Other Information
- Store below 43 C (110F)
- May discolor certain fabrics or surfaces
Inactive Ingredients
Distilled Water, Glycerin, Carbomer 940, Benzophenone-4, Aloe Vera, Aminomethyl Propanol.
Package Label - Principal Display Panel
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