NDC 55550-730 Antibiotic

NDC Product Code 55550-730

NDC 55550-730-21

Package Description: .9 g in 1 POUCH

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

NDC Product Information

Antibiotic with NDC 55550-730 is a product labeled by Total Resources International. The generic name of Antibiotic is . The product's dosage form is and is administered via form.

Labeler Name: Total Resources International

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.

  • MINERAL OIL (UNII: T5L8T28FGP)
  • PETROLATUM (UNII: 4T6H12BN9U)

Product Labeler Information

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

Labeler Name: Total Resources International
Labeler Code: 55550
Start Marketing Date: 10-07-2019 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: 12-31-2020 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.

Information for Patients

Neomycin Topical

Neomycin Topical is pronounced as (nee oh mye' sin)

Why is neomycin topical medication prescribed?
Neomycin, an antibiotic, is used to prevent or treat skin infections caused by bacteria. It is not effective against fungal or viral infections.This medication is sometim...
[Read More]

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Antibiotic 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

Other

Drug Facts

Active Ingredient (In Each Gram)

Neomycin Sulfate (3.5 mg Neomycin)

Purpose

First Aid Antibiotic

Use

First aid to help prevent infection in minor scrapes, cuts, and burns

Warnings

For external use only

Do Not Use

  • In eyes
  • Over large areas of the body or on puncture wounds, animal bites or serious burns
  • For more than 1 week unless directed by a doctor
  • If you are allergic to any of the ingredients

Stop Use And Ask A Doctor If

  • A rash or allergic reaction develops
  • Condition worsens or persists

Keep Out Of Reach Of Children

If ingested, contact a Poison Control Center right away.

Directions

  • Clean affected area
  • Apply a small amount 1 to 3 times daily
  • May cover with a sterile bandage

Inactive Ingredients

Mineral oil, petrolatum

* Please review the disclaimer below.