Active Ingredient
Benzalkonium Chloride 0.13%
Microsure Hand Sanitizer
FDA Label NDC 72513-000
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Strategia Project Management, Inc. for the product Microsure Hand Sanitizer (NDC 72513-000). 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 ingredient, purpose, uses:, warnings:, do not use, stop use and ask a doctor:, 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
Antimicrobial
Uses:
Sanitizes hands to helps reduce bacteria that potentially cause diseases.
Warnings:
For external use only.
Do Not Use
in eyes. If contact occurs, flush thoroughly with water.
Stop Use And Ask A Doctor:
If irritation or redness develops, or if condition persists for more than 72 hours.
Keep Out Of Reach Of Children:
If swallowed, get medical help or contact a Poison Control Center.
Directions:
Wipe on both hands to disinfect palms, between fingers, back of hands, and wrists. 8 hours of continues protection once skin is fully dry.
Inactive Ingredients:
Water, Hydrated Silica Complex
Package Labeling:72513-000-01
Label2 (Label2)
Package Labeling:72513-000-02
Label3 (Label3)
Package Labeling:72513-000-03
Label4 (Label4)
Package Labeling:72513-000-04
Label5 (Label5)
Package Labeling:72513-000-05
Label6 (Label6)
Package Labeling:72513-000-06
Label7 (Label7)
Package Labeling:72513-000-07
Label8 (Label8)
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