Active Ingredient(S)
Alcohol 70% v/v. Purpose: Antimicrobial
Sani-kure Extra Strength Hand Sanitizer
FDA Label NDC 78923-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Kolorcure Corporation for the product Sani-kure Extra Strength Hand Sanitizer (NDC 78923-001). 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(s), use:, warnings, do not use, otc - when using, directions, other information, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Use:
Antimicrobial
Warnings
Flammable. Keep away from heat or flame. Harmful if swallowed. For external use only.
Keep out of reach of children.
Do Not Use
in or around the eys.
Otc - When Using
In case of contact immediately flush eyes with water.
If swallowed, contact physician.
Keep out of reach of children.
Directions
- Place enough product in your palm to cover hands. Rub hands together until dry.
- Children under 6 years of age should be supervised when using Sani-Kure.
Other Information
Do not store above 110°F.
Inactive Ingredients
Pure Aloe Vera, vegetable glycerin, isopropyl alcohol, hydrogen peroxide, distilled water.
Package Label - Principal Display Panel
2 FL OZ (59 mL)
2 Oz Front Panel (2ozfrontsubmit)
2 Oz Drug Panel (2ozdrugpanelsubmit)
2 Oz Side Panel (2ozsidepanelsubmit)
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