Active Ingredients
Ethyl Alcohol 72%
My Medic Super Sanitizer Gel
FDA Label NDC 81417-008
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Sled Distribution, Llc for the product My Medic Super Sanitizer (NDC 81417-008). 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 ingredients, purpose, uses, warnings, otc - when using, otc - stop use, otc - keep out of reach of children, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Uses
- to decrease bacterica on the skin that could cause diease
- single use
Warnings
For external use only: Hands​
Flammable: Keep away from fire or flame.
Otc - When Using
When using this product
- Keep out of eyes. ln case of contact with eyes, flush thoroughly with water.
- Avoid contact with broken skin.
- Do not inhale or ingest.
Otc - Stop Use
Stop use and ask a doctor if
- irritation and redness develop.
- Condition persists 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 right away.
Directions
- Wet hands thoroughly with product and allow to dry without wiping.
- For children under 6, use only under adult supervision.
- Not recommended for infants.
Inactive Ingredients
Aloe Barbadensis Leaf Juice, Fragrance, Glycerin, Maltodextrin, Propylene Glycol, Triethanolamine Acrylates/C10-30 Alkyl Acrylate Cross Polymer, Water.
Package Label.Principal Display Panel
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