Antiseptic Hand Sanitizer
FDA Label NDC 72762-005
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 72762-005). 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, indications & usage, warnings, otc - keep out of reach of children, directions, storage and handling, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient
Alcohol 62%
Purpose
Antimicrobial
Indications & Usage
Uses ■ helps to reduce bacteria on the skin
■ recommended for repeated use
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.
Storage And Handling
Other information ■ do not store above 105°F
■ may discolor some fabrics or surfaces.
Inactive Ingredients
Fragrance, Glycerin, Propylene Glycol, Water
Packaging
Image (7276200516 1)
Image (72762 005 16 2)
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