Otc - Active Ingredient
Active Ingredient - 80% Ethyl Alcohol
Hand Sanitizer 60% Lv
FDA Label NDC 79107-323
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Sustainable Community Development, L.l.c. for the product Hand Sanitizer 60% Lv (NDC 79107-323). 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 otc - active ingredient, otc - purpose, warnings, otc - when using, otc - stop use, otc - keep out of reach of children, dosage & administration, inactive ingredient, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Uses: Helps reduce bacteria on the skin.
For use when soap and water are not available.
Warnings
For external use only.
Otc - When Using
When using this product:
Keep out of eyes.
In case of contact with eyes, flush thoroughly with water.
Avoid contact with broken skin
Otc - Stop Use
Stop use and call a doctor if irritation and redness develop and persist for more than 72 hours
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.
Dosage & Administration
Spray directly on hands and rub in thoroughly. For children under 6, use adult supervision. Not recommended for infants.
Inactive Ingredient
Glycerin, Hydrogen Peroxide, Organic Lavender Essential Oil, Purified Water
Indications & Usage
Uses: Helps reduce bacteria on the skin. For use when soap and water are not available.
Package Label.Principal Display Panel
130 mL NDC 79107-321-44
4.4 Oz Lavender Hand Sanitizer Label (Hand Sanitizer Lv Draft Xi 080520)
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