Dosage & Administration
Recommended for repeated use.
Hand Wipes
FDA Label NDC 72619-0820
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Accessory Myxx Llc for the product Hand Wipes (NDC 72619-0820). 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 dosage & administration, warnings, inactive ingredient, indications & usage, otc - keep out of reach of children, otc - purpose, otc - active ingredient, 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
Warnings
For external use only. Do not use over large areas of the body or if you are allergic to any of these ingredients.
When using this product avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation or redness develops and persists for more than 72 hours.
Keep out of reach of children.
If swallowed, get medical help or contact a Poison Control Center right away.
Inactive Ingredient
Water, Phenoxyethanol, Ethylhexylglycerin, Didecyldimonium Chloride , Propylene Glycol, Glycerin
Indications & Usage
Lift tab at front of the lid t o open.
Pull up corner of center sheet and thread
through di spenser slit i n the l id.
Pull up exposed wipe and snap off.
The next wipe i s ready for dispensing.
Close lid t o retain moisture.
Take wipe and rub thoroughly over all
surfaces of bot h hands. Rub hands briskly
together to dry.
Dispose of used wipe in trash.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children.
Otc - Purpose
For Hand Sanitizing to decrease bacteria on the skin. Recommended for repeated use.
Otc - Active Ingredient
Benzalkonium Chloride
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