Inactive Ingredient
Glycerol (1.45% V/v). Hydrogen Peroxide (0.125% V/v). Sterile Distilled Water Or Boiled Cold Water. (Inactive)
Hand Sanitizer
FDA Label NDC 73995-200
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Barley Creek Associates, L.p. for the product Hand Sanitizer (NDC 73995-200). 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 inactive ingredient, dosage & administration section, warning section, indications and usage section, indications and uses, otc - active ingredient, purpose section use, keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Warning Section
What The Captured Image Says! (Warnings4122020)
Purpose Section Use
Use(s): Hand Sanitizer To Help Reduce Bacteria That Potentially Can Cause Disease. For Use When Soap And Water Are Not Available. (Uses)
Other
All The Words That Go With It (Spl)
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