Instant Hand Sanitizer Bubble Gum
FDA Label NDC 53603-2002

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Bb17, Llc for the product Instant Hand Sanitizer Bubble Gum (NDC 53603-2002). 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 otc - active ingredient, otc - purpose, indications & usage, warnings, otc - stop use, otc - keep out of reach of children, dosage & administration, inactive ingredient, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Otc - Active Ingredient

Active ingredientsEthyl Alcohol 62% v/v

Otc - Purpose

PurposeAntimicrobial

Indications & Usage

KILLS MORE THAN 99.99% OF COMMON GERMS

Warnings

WARNING:Flammable, Keep away from fire or flame.  FOR EXTERNAL USE ONLY. DO NOT USE IN THE EYES.

Otc - Stop Use

DISCONTINUE USE IF IRRITATION AND REDNESS DEVELOP. IF CONDITION PERSISTS FOR MORE THAN 72 HOURS, CONSULT A DOCTOR.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children.

Dosage & Administration

DIRECTIONS:Rub into skin until dry. Other Information:Store below 110 F.

Inactive Ingredient

INACTIVE INGREDIENTS:Water, Aloe barbadenis, Leaf Juice, Glycerin,

Propylene Glycol, Carbomer, Triethanolamine, Fragrance, Tocopheryl Acetate, FD&C Red NO.33

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