NDC 77508-101 The Upper Hand

Ethyl Alcohol

NDC Product Code 77508-101

NDC 77508-101-02

Package Description: 59.15 mL in 1 BOTTLE

NDC 77508-101-04

Package Description: 118.2 mL in 1 BOTTLE

NDC 77508-101-08

Package Description: 236.5 mL in 1 BOTTLE, PUMP

NDC 77508-101-16

Package Description: 473.17 mL in 1 BOTTLE, PUMP

NDC 77508-101-28

Package Description: 3785.41 mL in 1 BOTTLE

NDC 77508-101-32

Package Description: 946.35 mL in 1 BOTTLE, PUMP

NDC 77508-101-64

Package Description: 1892.71 mL in 1 BOTTLE

NDC Product Information

The Upper Hand with NDC 77508-101 is a a human over the counter drug product labeled by Mi Medical Supply. The generic name of The Upper Hand is ethyl alcohol. The product's dosage form is gel and is administered via topical form.

Labeler Name: Mi Medical Supply

Dosage Form: Gel - A semisolid3 dosage form that contains a gelling agent to provide stiffness to a solution or a colloidal dispersion.4 A gel may contain suspended particles.

Product Type: Human Otc Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

The Upper Hand Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • ALCOHOL 70 mL/100mL

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • WATER (UNII: 059QF0KO0R)
  • SODIUM ACRYLOYLDIMETHYLTAURATE-ACRYLAMIDE COPOLYMER (1:1; 90000-150000 MPA.S) (UNII: 5F4963KLHS)
  • GLYCERIN (UNII: PDC6A3C0OX)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Mi Medical Supply
Labeler Code: 77508
FDA Application Number: part333A What is the FDA Application Number?
This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.

Marketing Category: OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final. What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Start Marketing Date: 06-01-2020 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2021 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.

Exclude Flag: N What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA’s requests for correction to deficient or non-compliant submissions. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

The Upper Hand Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling 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 flameFor External Use Only

Drug Facts Box Otc- When Using Section

When using this product do not use in or near the eyesIn 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

* Please review the disclaimer below.