Active Ingredient
Benzalkonium Chloride 0.13%
The following Structured Product Label (SPL) was submitted to the FDA by Target Corporation for the product Benzalkonium Chloride (NDC 82442-250). 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, do not use, when using this product, stop use and ask a doctor, keep out of reach of children., and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Benzalkonium Chloride 0.13%
Antimicrobial
For external use only.
if you are allergic to any of these ingredients.
avoid contact with eyes. In case of contact, flush eyes with water.
if irritation or redness develops, or if condition persists for more than 72 hours.
If swallowed, get medical help or contact Poison Control Center right away.
Water, Phenoxyethanol, Decyl Glucoside, Disodium EDTA, Sodium Benzoate, Potassium Sorbate, Vitamin E, Aloe Barbadensis Leaf Extract, Citric Acid, Fragrance
antibacterial
hand wipes
plant-based wipes
dermatologist tested
hypoallergenic
25 HAND WIPES
5½ IN X 8 IN
40 HAND WIPES
5½ IN X 8 IN
72 HAND WIPES
5½ IN X 8 IN
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