Active Ingredient
Ethyl Alcohol 62%
Antibacterial Hand Sanitizer Spray
FDA Label NDC 71513-202
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Broder Bros Co. for the product Antibacterial Hand Sanitizer (NDC 71513-202). 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 a doctor, 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
Uses
For hand sanitizing
Warnings
- Flammable.Keep away from heat and flame.
- For external use only.
When Using This Product
- Keep out of eyes
- In case of contact with eyes, flush thoroughly with water
- Avoid contact with broken skin
- Do not inhale or ingest
Stop Use And Ask A Doctor
if irritation and redness develops and persists for more than 72 hours
Keep Out Of Reach Of Children
If swallowed get medical help or call a Poison Control Center right away
Directions
- Wet hands thoroughly with product, briskly rub together until dry.
- Always supervise children in use of this product.
- Children under 6 months of age: Ask a doctor.
Other Information
Store at 66° to 77° F (22° to 25° C)
Inactive Ingredients
Aloe Barbadensis Leaf Extract, Carbomer, Deionizer Water, Fragrance, Glycerin, Propylene Glycol, Tocopherol Acetate, Triethanolamine
Questions?
1-800-873-7746 M-F 8 am - 5 pm EST
Other
Net wt. 10 mL/0.33 fl. oz.
Made in China
Dist. By Broder Bros Co., dba Prime Line
Gaffney, SC 29341
* Please review the disclaimer below.
