Active Ingredient
Benzalkonium Chloride 0. 13 %
Alcohol-free Hand Sanitizing Wipes 800ct
FDA Label NDC 75670-005
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Shanghai Sanjun General Merchandise Co., Ltd. for the product Alcohol-free Hand Sanitizing Wipes 800ct (NDC 75670-005). 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, otc - purpose, use, warning, 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
Otc - Purpose
Antiseptic
Use
●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.
Warning
●For extemal use only
●May iritate 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 up 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 dispensing up.
Inactive Ingredients
water, propylene glycol, disodium EDTA, chloro-methyl-isothiazolinone &
methyl-isothiazolinone, potassium sorbate, quaternium-15, aloe barbadensis leaf
juice, disodium cocoamphodiacetate, vitamin E acetate, polysorbate: 20, citric acid,
fragrance
Package Label.Principal Display Panel
1 (005)
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