Active Ingredient
BENZALKONIUM CHLORIDE .......... 0.13%
Antibacterial Wipes
FDA Label NDC 42129-030
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Fustin(xiamen) Commodity Co., Ltd for the product Antibacterial Wipes (NDC 42129-030). 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, warnings, indications & usage, otc - keep out of reach of children, directions, inactive ingredients, package label, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Warnings
For external use only.
When using this product. In case of contact with eyes, rinse thoroughly with water
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
Other information
Store in a cool dry place, away from direct sunlight and heat.
Indications & Usage
For hand cleaning to decrease bacteria on the skin. May be used on hands, arms and legs.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Directions
- For use apply thoroughly to hands and skin as desired.
- Discard wipe in trash receptacle after use.
- Do not flush.
- Keep the package opening securely shut to prevent the wipes from drying out.
Inactive Ingredients
Aloe Barbadensis Leaf Extract, Cetylpyridinium Chloride, Lonicera Japonica (Honeysuckle) Flower Extract, Polyaminopropyl Biguanide, Water
* Please review the disclaimer below.
