Kericure Hand Sanitizer Spray
FDA Label NDC 78280-304
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Kericure Inc. for the product Kericure Hand Sanitizer (NDC 78280-304). 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, packaging, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient
Alcohol 70% (v/v)
Purpose
Antimicrobial
Warnings
For external use only • Flammable, keep away from heat or flame • Do not use on children less than 2 month of age on open skin wounds • When using this product keep out of eyes, ears and mouth • In case of contact with eyes, rinse eyes thoroughly with water
Packaging
Image Description (Label2.1)
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