Active Ingredient(S)
Benzalkonium Chloride 0.13%
Sanitizing Hand Wipes
FDA Label NDC 51706-906
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Landy International for the product Sanitizing Hand Wipes (NDC 51706-906). 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(s), purpose, use, warnings, otc - keep out of reach of children, directions, inactive ingredients, package label - 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/Hand & Skin Sanitizer
Use
Sanitizing Hand Wipes to help decrease bacteria on the skin.
Recommended for single use.
Warnings
Do not freeze. For external use only.
Do not use in ears, eyes or mouth.
●Avoid contact with the eyes. In case of contact, flush eyes with water.
●Stop use and ask a doctor if redness or iritation
develop and persist for more than 72 hours.
●Keep out of reach of children.
●Children should be supervised when using this product.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children.
Directions
Wipe liberally over the hands & body, rub into skin until dry.
Recommended for single use.
Inactive Ingredients
Aloe Barbadensis leaf extract, Aqua, Citric Acid, CaprylyI Glucoside,
Laureth-4, Polyhexanide, Phenoxyethanol, Triethoxysilylpropyl
Steardimonium Chloride.
Package Label - Principal Display Panel
1 (906)
* Please review the disclaimer below.
