Active Ingredient
Benzalkonium Chloride 0.13%
Defender Wipe
FDA Label NDC 78411-002
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Zhejiang Qirun Daily Necessities Co., Ltd. for the product Defender Wipe (NDC 78411-002). 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, use, warning, otc - keep out of reach of children, directions, 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
Use
For hand sanitizing to decrease bacteria on the skin.
Warning
For external use only
May irritate eyes
Keep out reach of children unless under adult supervision
Otc - Keep Out Of Reach Of Children
Keep out of reach of children unless under adult supervision
Directions
Tear V notch located on top of the plastic bag.
Pull out the first wipe approoirmately 6 to 8 inches from the center of the rol.
Place entire bag inside of center pull dispenser,
Thread the wipe through the opening on the dispenser,
Closo the id of the disponser. Wipe dispensing tension may be adjusted on tho top of
dispenser. Dispenser must be mounted with wipes desponsing up.
Apply topically to the skin to help prevent cross contamination.
Recommended for repeated use.
Dries in seconds.
Inactive Ingredients
Aloe Barbadensis Leaf Juice, Aqua,Parfum, Phenoxyethanol, Propylene Glycol, Polysorbate 20,Tocopheryl Acetate
* Please review the disclaimer below.
