Active Ingredient
Benzalkonium Chloride 0.13% w/w
Antiseptic Wipe
FDA Label NDC 55550-225
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Total Resources International for the product Antiseptic Wipe (NDC 55550-225). 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, 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
Antimicrobial
Uses
for handwashing to decrease bacteria on the skin
Warnings
For external use only
When using this product avoid contact with eyes. If in eyes flush thoroughly with water
Discontinue use and contact a doctor if irritation and redness develop and conditions persist for more than 72 hours
Keep Out Of Reach Of Children
Keeo out of reach of children. If swallowed, get medical help or contact Poison Control Center immediately.
Directions
- remove and unfold wipe
- wipe hands thoroughly and allow hands to air dry
- do not flush
Other Information
Store at room temperature
Inactive Ingredients
Aloe Barbadensis Leaf Juice, Citric Acid, Glycerin, Hamamelis Virginiana (Witch Hazel) Bark/Leaf/Twig Extract, Phenoxyethanol, Polysorbate 20, Tocopheryl Acetate, Water
Label
Label (Aaa)
ANTISEPTIC WIPE
BE SMART GET PREPARED
KILLS 99.9% OF GERMS
- ​ALOE VERA
- VITAMIN E
- ANTIBACTERIAL
- Made in USA
- Manufactured for: TOTAL RESOURCES INTL.
- Walnut, California 91789
- 00-TOW-94186 Rev.00
- NDC# 55550-225-11
1 PC, Pre- moistened Wipe, SINGLE USE
* Please review the disclaimer below.
