Active Ingredient
Ethyl Alcohol 70% v/v
Pigeon Hand Sanitizer
FDA Label NDC 78151-010
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Pigeon Corporation for the product Pigeon Hand Sanitizer (NDC 78151-010). 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, inactive ingredient, purpose, warnings, keep out of reach of children, uses:, directions, other information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Inactive Ingredient
Water, Butylene Glycol, Carbomer, Triethanolamine, Citrus Paradisi (Grapefruit) Fruit Extract, Citrus Limon (Lemon) Fruit Extract, Camellia Sinensis Leaf Extract
Purpose
Hand Sanitizer
Warnings
Flammable. Keep away from fire or flame.
For external use only
When using this product do not use in or near the eyes.
In case of contact, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation or rash appears and lasts.
Keep Out Of Reach Of Children
If swallowed, get medical help
Uses:
Hand sanitizer to help reduce bacteria on the skin
Directions
Put enough product in your palm to cover hands and rub hands together briskly until dry.
Children under 6 years of age should be supervised when using PIGEON
Other Information
Store below 90°F (32.2°C)
* Please review the disclaimer below.
