Active Ingredients
Alcohol 70%
Hand Sanitizer
FDA Label NDC 73659-007
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Rapid Care, Inc for the product Hand Sanitizer (NDC 73659-007). 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 ingredients, purpose, uses, warnings, do not use, 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
Purpose
Antiseptic
Uses
- for handwashing to decrease bacteria on skin without soap and water.
- recommended for repeated use
Warnings
For external use only.
Flammable, keep away from fire or flames.
Do not use in the eyes. If this happens, rinse thoroughly with water.
Use with caution if allergic to alcohol.
Do Not Use
in the eyes. If this happens, rince thoroughly with water
Stop Use And Ask A Doctor If
irritation and redness develop and persists for more than 72 hours
Keep Out Of Reach Of Children.
If ingested get medical help or contact a Poison Control Center right away
Directions
- wet hands and wrists thoroughly with product and allow to dry without wiping
- children under 6 years of age should be supervised while using this product
Inactive Ingredient
carbomer, favor, glycerine, triclosen, triethanolamine, purified water
* Please review the disclaimer below.
