Active Ingredient
BENZALKONIUM CHLORIDE 0.1%
Antibacterial Wet Wipes
FDA Label NDC 81472-101
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Runmei Paper (fujian) Co., Ltd. for the product Antibacterial Wet Wipes (NDC 81472-101). 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, warning, otc - keep out of reach of children, directions of use, 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
Uses
FOR HAND WASHING TO DECREASE BACTERIA ON THE SKIN. RECOMMENDED FOR REPEAT USE.
Warning
- For external use only
- Keep out of reach of eyes. If contact occurs, rinse throughtly with water.
- Do not use if you are allergic to any of the ingredients.
- Discontinue use if irritation or redness develops, and if condition persists for more than 72 hours consult a physician.
- Keep out of reach of children unless under adult supervision.
- If swollowed, get medical help, or contact a Poison Control Center immediately.
Otc - Keep Out Of Reach Of Children
KEEP OUT OF REACH OF CHILDREN UNLESS UNDER ADULT SUPERVISION.
IF SWALLOWED, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER IMMEDIATELY.
Directions Of Use
Open resealabel label pull one sheetfrom pack. Thoroughly clean hands or affected area and discard in receptacle, and do not flush. Allow to dry without wiping. Be sure to reseal label complete to retain moisture.
Inactive Ingredients
Water, Opuntia Streptacantha stem Extract, Ethylhexylglycerin, Propylene Glycol, Benzethonium Chloride, Polyaminopropyl Biguanide
* Please review the disclaimer below.
