Active Ingredient:
Alcohol 80% v/v
Alcohol Antiseptic 80
FDA Label NDC 77188-000
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Resource One Inc for the product Alcohol Antiseptic 80 (NDC 77188-000). 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 active ingredient:, purpose:, use(s):, warnings:, when using this product:, stop and ask a doctor if:, 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
Purpose:
Antiseptic
Use(S):
Hand sanitizer to help reduce the bacteria that potentially will cause disease
Warnings:
For External Use Only
Flammable keep away from children
When Using This Product:
Keep out of eyes, ears, and mouth. In case of contact with eyes, rinse thoroughly with water.
Stop And Ask A Doctor If:
If irration 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:
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:
Glycerin, Hydrogen peroxide, purified water USP
Packaeg Labeling:
Bottle (Bottle)
* Please review the disclaimer below.
