Antiseptic Hand Sanitizer
FDA Label NDC 72762-006

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Two's Company, Inc. for the product Antiseptic Hand Sanitizer (NDC 72762-006). 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, purpose, warnings, otc - keep out of reach of children, directions, inactive ingredients, packaging, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Drug Facts

Active Ingredient

Alcohol 62%

Purpose

Antimicrobial

Warnings

For external use only

Flammable: Keep away from heat and flame

When using this product

do not use in or near the eyes. In case of eye contact, rinse eyes thoroughly with water ■ do not apply to irritated or broken skin.

Stop use and ask a doctor if ■ irritation and redness develop ■ condition persists for more than 72 hours.

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.

Directions

■ lift tab and spray a small amount into the palms of your hands and forearms.

■ wet the hands thoroughly with product, rub hands together and allow to dry without wiping ■ no rinsing required.

■ children under 6 years of age should be supervised when using this product ■ not recommended for infants.

Inactive Ingredients

Fragrance, Glycerin, Propylene Glycol, Water

Packaging

Image (7276200616 15)

Image (7276200616 15)

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