Active Ingredient
BENZALKONIUM CHLORIDE 0.1% (ANTISEPTIC)
Foaming Hand Sanitizer
FDA Label NDC 37808-240
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Heb for the product Foaming Hand Sanitizer (NDC 37808-240). 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, uses and directions, warnings, when using this product, stop use and ask a doctor if, keep out of reach of children, package front and back labels, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Uses And Directions
- USES: TO HELP REDUCE BACTERIA ON THE SKIN THAT COULD CAUSE DISEASE. RECOMMENDED FOR REPEATED USE.
- DIRECTIONS: PUMP ENOUGH PRODUCT TO YOUR PALM TO THOROUGHLY COVER YOUR HANDS, RUB TOGETHER UNTIL DRY.
Warnings
- FOR EXTERNAL USE ONLY.
When Using This Product
- AVOID CONTACT WITH EYES. IF CONTACT OCCURS, RINSE EYES WITH WATER.
Stop Use And Ask A Doctor If
- SKIN IRRITATION OR REDNESS DEVELOPS AND LASTS.
Keep Out Of Reach Of Children
- IN CASE OF ACCIDENTAL INGESTION, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER IMMEDIATELY.
Package Front And Back Labels
- 8OZ FRONT AND BACK LABELS: hcf8.jpg
8oz Front And Back Labels (Hcf8)
* Please review the disclaimer below.
