Active Ingredient
Benzalkonium Chloride 0.13%
Benzalkonium Chloride
FDA Label NDC 67151-323
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Progressive for the product Benzalkonium Chloride (NDC 67151-323). 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, otc - keep out of reach of children, directions, inactive ingredients, principal display panel, 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 to decrease bacteria on the skin.
- Apply topically to the skin to help prevent cross contamination.
- Recommended for repeated use.
- Dries in seconds.
Warnings
For external use only.
May irritate eyes.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children unless under adult supervision
Directions
- Tear V notch on top of plastic bag.
- Pull first wipe from the center of roll through opening of bag.
- Thread first wipe through the dispensing nozzle in lid of floor stand or
- Thread first wipe through the dispensing nozzle in top of wall mounted dispenser.
- Close dispenser door. Wipe dispensing tension may be adjusted on top of dispenser. Dispenser must be mounted with wipes disepensing up.
Inactive Ingredients
Aloe Barbadensis Leaf Juice, Tocopherol Acetate, Sodium Hydroxide, Dehydroacetic Acid, Tetrasodium EDTA, Benzoic Acid, PEG 40 Hydrogenated Castor Oil, Benzalkonium Chloride, Cocamidapropyl Betaine, Fragrance, Propylene Glycol, Phenoxyethanol, Water.
Principal Display Panel
wipes plus
SANITIZING ALCOHOL FREE WIPES
- Kills 99.9% of germs
800 CT
* Please review the disclaimer below.
