Boogie Hands Antibacterial Wet Wipes Cloth
FDA Label NDC 79747-014

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Eleeo Brands Llc for the product Boogie Hands Antibacterial Wet Wipes (NDC 79747-014). 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 ingredients, purpose, use, warnings, do not use, when using this product, stop use and ask a doctor if, 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

Active Ingredients

Benalkonium chloride (0.13%)

Purpose

Antimicrobial

Use

For hand sanitizing to decrease bacteria on skin

Warnings

For external use only

Do Not Use

if you are allergic to any of the ingredients

When Using This Product

avoid contact with the eyes. In case of eye contact, flush eyes with water.

Stop Use And Ask A Doctor If

if irritation or redness develops.

Keep Out Of Reach Of Children.

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

Directions:

  • Rub wipe over all surfaces of both hands. Wet hands thoroughly with wipe.

    • Allow to dry without wiping.

      • Children under 2 years of age:ask doctor prior to use.

        • Children under 6 years of age:use adult supervision.

Inactive Ingredients

Purified water, Decyl glucoside, Aloe barbadensis(aloe) leaf extract, Tocopheryl (Vitamin E) acetate, Disodium EDTA, Potassium sorbate, Sodium benzoate, Phenoxyethanol, Citric acid, Fragrance

Principal Display Panel

20ct NDC:79747-014-02

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