Active Ingredient
ETHYL ALCOHOL 62%
Antibacterial
FDA Label NDC 37808-235
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by H E B for the product Antibacterial (NDC 37808-235). 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, when using this product, stop use and ask doctor, keep out of the 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
ANTIBACTERIAL
Uses
TO DECREASE THE BACTERIA ON THE SKIN
Warnings
FOR EXTERNAL USE ON THE HANDS ONLY. IN CASE OF ACCIDENTAL INGESTION SEEK MEDICAL ASSISTANCE OR CONTACT A POISON CONTROL CENTER IMMEDIATELY.
When Using This Product
AVOID CONTACT WITH EYES. IF EYE CONTACT OCCURS, FLUSH THOROUGHLY WITH WATER. AVOID CONTACT WITH BROKEN SKIN.
Stop Use And Ask Doctor
IF SKIN IRRITATION DEVELOPS
Keep Out Of The Reach Of Children
FOR CHILDREN UNDER 6, USE ONLY WITH ADULT SUPERVISION. NOT RECOMMENDED FOR USE ON INFANTS.
Directions
SPRAY A SMALL AMOUNT ONTO HANDS AND BRISKLY RUB HANDS TOGETHER UNTIL DRY
Other Information
FLAMMABLE. KEEP AWAY FROM HEAT AND FLAME.
Inactive Ingredients
WATER, PROPYLENE GLYCOL, GLYCERIN, FRAGRANCE, ISOPROPYL MYRISTATE, TOCOPHERYL ACETATE.
Label Copy
Image Of The Label (Hcf01)
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