The Upper Hand
FDA Label NDC 77508-101
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Mi Medical Supply for the product The Upper Hand (NDC 77508-101). 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 the upper hand gel sanitizer, drug facts box, drug facts box otc- purpose section, drug facts box otc- indications and usage section, drug facts box otc - warnings section, drug facts box otc- when using section, drug facts box otc- stop use section, drug facts box otc- keep out of reach of children section, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Drug Facts Box
Ethyl Alcohol 70%
Drug Facts Box Otc- Purpose Section
Antiseptic
Drug Facts Box Otc- Indications And Usage Section
Hand Sanitizer to help reduce bacteria on the skin that could cause disease.
Recommended for Repeated use
Drug Facts Box Otc - Warnings Section
Flammable, Keep away from fire or flame
For External Use Only
Drug Facts Box Otc- When Using Section
When using this product do not use in or near the eyes
In case of contact, rinse eyes thoroughly with water
Drug Facts Box Otc- Stop Use Section
Stop use and ask a doctor if irritation or rash appears and lasts
Drug Facts Box Otc- Keep Out Of Reach Of Children Section
Keep out of reach of children. If swallowed, get medical help or contact a poison control center right away.
Drug Facts Box Otc-Dosage And Administration Section
Wet hands thoroughly with product and allow to dry without wiping.
Drug Facts Box Otc- Inactive Ingredient Section
Glycerin, Water, Polyacrylamide, C13-14 Isoparrafin, Laureth-7
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