Active Ingredient(S)
Benzalkonium Chloride 0.13%
Hand Sanitize Wipes
FDA Label NDC 51706-958
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 Hand Sanitize Wipes (NDC 51706-958). 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, other information, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Use
Uses santizing hand wipes to help decrease bacteria on the skin.recommended for single use.
Warnings
For external use only
Do not use if you are allergic to any of the ingredients.
When using this product do not get into eyes. If contact occurs, flush eyes in water.
stop use and ask a doctor if irritation develops and condition for more than 72 hours.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. Children should be supervised when using this product.
Directions
Directions wipe liberally over the hands & body, rub into skin until
Other Information
- Other information Do not store above 110°F(43℃).
Inactive Ingredients
aloe extract, glycerin, phenoxyethanol, purified water
Package Label - Principal Display Panel
1 (958)
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