Active Ingredients
Benzalkonium Chloride 0.13%
Benzalkonium Chloride
FDA Label NDC 67151-313
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 67151-313). 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 ingredients, purpose, uses, warnings, otc - keep out of reach of children, directions, inactive ingredient, 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
- Remove lid
- Pull wipe from center of roll and thread through opening in lid
- Replace lid, pull wipe up, and then out 45° angle
- Close lid to retain moisture
Do not push finger through opening
The next wipe dispenses automatically
Inactive Ingredient
Aloe Barbadensis Leaf Juice, Disodium EDTA, DMDM Hydantoin, Ethylparaben, Fragrance, Methylparaben, Phenoxyethanol, Polysorbate 20, Sodium Citrate, Water
Principal Display Panel
wipesplus
HAND SANITIZING
alcohol wipes
lemon scent
Kills 99.9% of germs
* Please review the disclaimer below.
