Sani Hands
FDA Label NDC 79359-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Maine Craft Distilling, Llc for the product Sani Hands (NDC 79359-001). 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 drug facts, active ingredient, purpose, uses, directions, warnings, otc - keep out of reach of children, other information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient
Ethyl Alcohol 72%
Purpose
Antiseptic
Uses
Hand Sanitizer to help reduce bacteria on the skin that can cause disease.
Directions
Apply liberally to front and back of hands.
Allow to dry. Recommended for repeat use.
Warnings
For external use only: hands
Flammable, keep away from fire or flame.
When using this product avoid contact with the eyes. In case of contact, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation or redness appears and lasts.
Do not use on children less than 2 months of age and on open wounds. Do not inhale or ingest.
Supervise children under 6 years of age when using this product to avoid swallowing
Otc - Keep Out Of Reach Of Children
If swallowed, get medical help or contact a Poison Control Center immediately.
Other Information
Store between 0°C (32°F) - 41°C (105°F)
Inactive Ingredients
Methylcellulose, water, Fragrance
Customer Service
+1 800 960 4814
Packaging
Image (7935900116)
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