Active Ingredient(S)
Benzalkonium Chloride 0.13mg in 100mL
Alcohol-free Sanitizing Wipes
FDA Label NDC 40562-010
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Anhui Hanbon Daily Chemical Co., Ltd. for the product Alcohol-free Sanitizing Wipes (NDC 40562-010). 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(s), purpose, use, warnings, do not use, otc - when using, otc - stop use, otc - keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antibacterial
Use
For hand washing to decrease bacteria on the skin.
Warnings
For external use only.
Do Not Use
- in the eyes.
- if you are allergic to any of the ingredients.
Otc - When Using
If eye contact occurs, rinse thoroughly with water.
Otc - Stop Use
If irritation or redness develops and persist for more than 72 hours.
Otc - Keep Out Of Reach Of Children
If swallowed, get medical help or contact a Poison Control Center right away.
Directions
- Storage. Store at room temperature.
- Dispensing. Peel back from label. Remove wipe(s). Reseal by pressing label over opening.
- Use. Apply wipe thoroughly to hands as desired. Allow to dry without wiping.
- Disposal. Dispose of used wipes in trash receptacle after use. Do not flush.
Inactive Ingredients
Water, Glycerin, Phenoxyethanol, Aloe Barbadensis Leaf Extract, Polysorbate 20, Polyaminopropyl Biguanide, 2-bromo-2-nitropropane-1,3-diol, Tocopheryl Acetate, Citric Acid.
Package Label - Principal Display Panel
20 PATCH in 1 PACKET NDC: 40562-010-01
20pcs Label (20)
* Please review the disclaimer below.
