Active Ingredient
Ethyl Alcohol 62%
Antibacterial
FDA Label NDC 49794-010
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Continental Manufacturing Chemist, Inc. for the product Antibacterial (NDC 49794-010). 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, purpose, use(s), for external use only, stop use and ask a doctor if, keep out of reach of children, directions, storage, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Use(S)
To decrease bacteria on skin
For External Use Only
Flammable! Keep away from fire or flame. Do not use in eyes; if this happens rinse thoroughly with water.
Stop Use And Ask A Doctor If
irritation or redness develops and persists more than 72 hours.
Keep Out Of Reach Of Children
If ingested get medical help or contact a Poison Control Center right away
Directions
Wet hands thoroughly with product and allow to dry without wiping. Children under six should be supervised when using this product.
Storage
Do not store above 105F (40C)
Inactive Ingredients
Amino Methyl Propanol, Carbomer, Propylene Glycol, Purified Water
Principal Display Panel
Antibacterial Spray Bulk Package Labels (Antibacterial 1)
* Please review the disclaimer below.
