Hand Sanitizer W/carabiner
FDA Label NDC 76138-104

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Innovation Specialties for the product Hand Sanitizer W/carabiner (NDC 76138-104). 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, otc - keep out of reach of children, indications & usage, warnings, dosage & administration, inactive ingredient, otc - questions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Otc - Active Ingredient

Active Ingredient

Ethyl Alcohol 62%

Otc - Purpose

Purpose

Antiseptic

Otc - Keep Out Of Reach Of Children

Keep out of reach of children If swallowed get medical help or contact a Poison Control Center right away.

Indications & Usage

Directions

Spread on both hands, rub in, let dry.

Warnings

Warnings

Flammable, keep away from fire or flame, For external use only.

Dosage & Administration

Spread on both hands, rub in, let dry.

Inactive Ingredient

Inactive Ingredients

Aloe Barbadensis Gel, Carbomer, Fragrance, Glycerin, Propylen Glycol, Tocopheryl Acetate, Triethanolamine, Water.

Otc - Questions

Questions ?

Call 1-855-755-5346

Package Label.Principal Display Panel

Product Label (5254)

Product Label (5254)

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