Dewmed Wet Wipes Antibacterial
FDA Label NDC 80065-003

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Dewmed, Llc for the product Dewmed Wet Wipes Antibacterial (NDC 80065-003). 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 drug facts, active ingredient, uses, warnings, when using this 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.

Drug Facts

Active Ingredient

Benzalkonium Chloride 0.13%

Uses

To help reduce bacteria that potentially can cause disease.

Warnings

  • For external use only.

When Using This Product

  • do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

Stop Use And Ask A Doctor

if irritation or rash appears.

Keep Out Of Reach Of Children.

If swallowed, get medical help or contact a Poison Control Center

Directions

Thoroughly wipe hands with wipe. Discard in trash receptacle; do not flush. Be sure to reseal label complete to retain moisture.

Inactive Ingredients

Aqua, Phenoxyethanol, Cocamidopropyl Betaine, Glycerin, PEG-40 Hydrogenated Castor Oil, Disodium EDTA, Parfum.

Package Labeling:

Bottle (Bottle)

Bottle (Bottle)

* Please review the disclaimer below.