Baturals Hand Sanitizer
FDA Label NDC 74218-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Guangdong Authenmole Biotech Inc. for the product Baturals Hand Sanitizer (NDC 74218-001). 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, indications & usage, warnings, otc - keep out of reach of children, dosage & administration, storage and handling, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient
Ethyl alcohol 75%
Purpose
Antiseptic
Indications & Usage
Use ▪ Helps decrease bacteria on skin. ▪ Recommended for repeated use.
Warnings
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 redness develops.
Otc - Keep Out Of Reach Of Children
Keep Out of Reach of Children. If swallowed, get medical help or contact a Poison Control Center right away.
Dosage & Administration
Directions ▪ Place enough product in your palm to thoroughly cover your hands
▪ Rub hands together briskly until dry
▪ Children under 6 years of age use only under adult supervisions
Storage And Handling
Other information ▪ Store at 77°F (25°C) ▪ May discolor fabrics
Inactive Ingredients
Water, Propylene, Glycerin, Fragrance, Carbomer, Triethanolamine, Tocopheryl Acetate
Other
Kills 99.9% of Germs
Refreshing Gel
Packaging
Image Description (Baturals)
* Please review the disclaimer below.
