Hand Sanitizer Gel
FDA Label NDC 80689-000
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Hygieia for the product Hand Sanitizer (NDC 80689-000). 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 drug facts, active ingredient, purpose, use, warnings, when using this product, keep out of reach of children, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient
Alcohol 75%
Purpose
Antiseptic
Use
For hand sanitizing
Warnings
For external use only
Flammable, keep away from fire & flames.
When Using This Product
- Avoid the eyes and mucous membranes.
- In case of contact, rinse area thoroughly with water
- Do not drink. If taken internally will produce serious gastric disturbances
Keep Out Of Reach Of Children
If swallowed contact a doctor or Poison Control Center immediately
Directions
Rub dime sized amount between hands until dry
Other Information
- Store below 105 °F
- May discolor some fabrics
Inactive Ingredients
Water, Glycerin, Propylene Glycol, Carbomer, Aminomethyl Propanol.
Package Labeling:
Bottle (Bottle)
* Please review the disclaimer below.
