Foaming Hand Sanitizer Liquid
FDA Label NDC 83986-118

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Uplift Brands Llc for the product Foaming Hand Sanitizer (NDC 83986-118). 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, warnings, when using this product, stop use and ask a doctor if, keep out of reach of children., directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

→ Active Ingredient

→ Purpose

→ Use

→ Warnings

→ When Using This Product

→ Stop Use And Ask A Doctor If

→ Keep Out Of Reach Of Children.

→ Directions

→ Inactive Ingredients

→ Claims

→ Adverse Reactions

→ Principal Display Panel

Active Ingredient

Benzalkonium Chloride 0.13%

Purpose

Antiseptic

Use

to decrease bacteria on the skin

Warnings

For external use only: hands only

When Using This Product

keep out of eyes. In case of contact with eyes, flush thoroughly with water.
avoid contact with broken skin

Stop Use And Ask A Doctor If

if irritation and redness develop
condition persists for more than 72 hours

Keep Out Of Reach Of Children.

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

Directions

wet hands thoroughly with product and allow to dry without wiping
for children under 6, use only under adult supervision
not recommended for infants

Inactive Ingredients

cetrimonium chloride, diglycerin, disodium cocoamphodiacetate, fragrance, glycerin, hydrochloric acid, methoxy PEG/PPG-7/3 aminopropyl dimethicone, sodium benzoate, tetrasodium EDTA, water