NDC 62257-773 Medisoft

  1. Labeler Index
  2. Abc Compounding Co., Inc.
  3. NDC: 62257-773 Medisoft

NDC Product Code 62257-773

NDC CODE: 62257-773

Proprietary Name: Medisoft What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
Non-Proprietary Name: What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

NDC Code Structure

NDC 62257-773-25

Package Description: 199 g in 1 CAN

NDC 62257-773-26

Package Description: 454 g in 1 CAN

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Medisoft with NDC 62257-773 is a product labeled by Abc Compounding Co., Inc.. The generic name of Medisoft is . The product's dosage form is and is administered via form.

Labeler Name: Abc Compounding Co., Inc.

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.
  • PROPANE (UNII: T75W9911L6)
  • BUTANE (UNII: 6LV4FOR43R)
  • WATER (UNII: 059QF0KO0R)

Product Labeler Information

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

Labeler Name: Abc Compounding Co., Inc.
Labeler Code: 62257
Start Marketing Date: 08-31-2009 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: 12-31-2018 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: I - INACTIVATED, the listing data was inactivated by the FDA. 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 ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".

* Please review the disclaimer below.

Medisoft Product Label Images

Medisoft 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 Otc-Active Ingredients Section

Ethyl Alcohol 62%

Drug Facts Box Otc-Purpose Section

Antiseptic

Drug Facts Box Otc-Indications And Usage Section

For hand-washing to decrease bacteria on the skin, only when water is not available

Drug Facts Box Otc-Warnings Section

Flammable, keep away from fire and flamesFor external use only

Drug Facts Box Otc-When Using Section

Do not get into eyesif contact occurs, rinse eyes thoroughly with water

Drug Facts Box Otc-Stop Use Section

Irritation and redness develop

Drug Facts Box Otc-Keep Out Of Reach Of Children Section

If swallowed, get medical help or contact a Poison Control Center right away

Drug Facts Box Otc-Dosage & Administration Section

Press valve once to deliver one squirt (about a quarter size) of foaming product onto the palm of your handrub hands together and allow to dry without wiping

Drug Facts Box Otc-Inactive Ingredients Section

Water, DEA-C8-18 perfluoroalkylethyl phosphate, cetearyl alcohol, polysorbate 65, dimethicone PEG-8 meadowfoamate, meadowfoamamidopropyl betaine, butane, propane, fragrance

Medisoft 4773 199G

477307PA.jpg  MediSoft  199g

* Please review the disclaimer below.