Active Ingredient
Benzalkonium
Chloride 0.125%
Antibacterial Hand Wipes
FDA Label NDC 77070-702
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Goodfibers for the product Antibacterial Hand Wipes (NDC 77070-702). 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, warnings, when using product, stop use and ask a doctor, keep out of reach of children, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antimicrobial
Uses
*For hand washing to decrease bacteria on skin without requiring water or rinsing.
*Recommended for repeated use
Warnings
For external use only.
When Using Product
*Do not use in or near eyes.
If contact occurs, rinse eyes thoroughly with water.
Stop Use And Ask A Doctor
*If irritation and redness persist for more than 72 hours.
Keep Out Of Reach Of Children
In case of accidental indestion, seek medical attention or contact a poison control center immediately.
Directions
*Wet thoroughly hands with wipe and allow to dry without wiping.
*Children under six years of age should be supervised when using this product.
Inactive Ingredients
Aloe Barbadensis Leaf Juice, Citric Acid, Decyl Glucoside, Fragrtance, Phenoxyethanol, Potassium Sorbate, Tetrasodium EDTA, Water.
Pdp
MEDIC THERAPEUTICS
ANTIBACTERIAL
HAND WIPES
___________________
KILLS 99.9% OF GERMS
Sanitize on the Go
Active Ingredient -
Benzalkonium Chloride (0.125%)
7 x 5.1in (18 x 13 cm)
20 CT
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