NDC 69396-072 Multi Action

Bacitracinzinc, Neomycinsulfate, Polymyxinbsulfate, Pramoxinehcl

NDC Product Code 69396-072

NDC CODE: 69396-072

Proprietary Name: Multi Action 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: Bacitracinzinc, Neomycinsulfate, Polymyxinbsulfate, Pramoxinehcl 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.

Drug Use Information

Drug Use Information
The drug use information is a summary and does NOT have all possible information about this product. This information does not assure that this product is safe, effective, or appropriate. This information is not individual medical advice and does not substitute for the advice of a health care professional. Always ask a health care professional for complete information about this product and your specific health needs.

  • Drug uses not available
  • This medication is used to decrease the risk of infection after certain intestinal surgeries. Neomycin belongs to a class of drugs known as aminoglycoside antibiotics. It works by stopping the growth of bacteria in the intestines. Neomycin may also be used along with a special diet to treat a certain serious brain problem (hepatic encephalopathy). This condition is caused by too much of a certain natural substance (ammonia). Normally, the liver gets rid of ammonia, but liver disease can cause too much ammonia to build up in the body. This medication helps treat encephalopathy by killing certain intestinal bacteria that make ammonia. This antibiotic treats only bacterial infections. It will not work for viral infections (such as common cold, flu). Using any antibiotic when it is not needed can cause it to not work for future infections.

NDC Code Structure

  • 69396 - Trifecta Pharmaceutical Usa Llc

NDC 69396-072-01

Package Description: 1 TUBE in 1 BOX > 28.4 g in 1 TUBE

NDC Product Information

Multi Action with NDC 69396-072 is a a human over the counter drug product labeled by Trifecta Pharmaceutical Usa Llc. The generic name of Multi Action is bacitracinzinc, neomycinsulfate, polymyxinbsulfate, pramoxinehcl. The product's dosage form is ointment and is administered via topical form.

Labeler Name: Trifecta Pharmaceutical Usa Llc

Dosage Form: Ointment - A semisolid3 dosage form, usually containing <20% water and volatiles5 and >50% hydrocarbons, waxes, or polyols as the vehicle. This dosage form is generally for external application to the skin or mucous membranes.

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.

Multi Action 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.

  • POLYMYXIN B SULFATE 10000 [USP'U]/g
  • BACITRACIN ZINC 500 [USP'U]/g
  • NEOMYCIN SULFATE 3.5 mg/g
  • PRAMOXINE HYDROCHLORIDE 10 mg/g

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.

  • PYRUVIC ACID (UNII: 8558G7RUTR)
  • ALPHA-TOCOPHEROL (UNII: H4N855PNZ1)
  • OLIVE OIL (UNII: 6UYK2W1W1E)
  • PETROLATUM (UNII: 4T6H12BN9U)
  • LEVANT COTTONSEED OIL (UNII: N5CFT140R8)
  • COCOA BUTTER (UNII: 512OYT1CRR)

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.

Product Labeler Information

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

Labeler Name: Trifecta Pharmaceutical Usa Llc
Labeler Code: 69396
FDA Application Number: part333B 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 FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph. 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: 01-22-2021 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: 12-31-2022 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’.

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Multi Action Product Label Images

Multi Action 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

Active Ingredient

Bacitracin Zinc 500 Units

Neomycin Sulfate 3.5mg

Polymyxin B Sulfate 10,000 Units

Pramoxine HCL 10mg

Purpose

First Aid Antibiotic

First Aid Antibiotic

First Aid Antibiotic

Pain Reliever

Uses

Helps prevent infection in and temporarily relieves pain due to minor cuts, scrapes and burns.

Warnings

  • For external use only. Do not use:If you are allergic to any of the ingredientsin or near the eyeson large areas of the body

Ask A Doctor Before Use

  • Ask Doctor before use if you have:Deep or puncture woundsAnimal bitesSerious burns

Stop Use And Ask A Doctor If:

  • Condition persists or gets worseSymptoms last for more than 7 days or clear up and come back within a few daysA rash or other allergic reaction develops

When Using This Product

Do not use longer than 1 week

Keep Out Of Reach Of Children

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

Directions

  • Adults and children 2 years and older:Clean the affected areaApply a small amount of this product (an amount equal to the surface area of the tip of a finger) on the area 1 to 3 times dailyMay be covered with a sterile bandageChildren under 2 years: ask a doctor

Other Information

  • To Open: Unscrew cap, pull tab to remove foil sealStore at 20° to 25°C (68° to 77°F)See carton or tube crimp for lot number and expiration date

Distributed ByTrifecta Pharmaceuticals USA®101 NE Third Avenue, Suite 1500Ft. Lauderdale, FL. 33301 USAProduct of PRCwww.trifecta-pharma.comThis product is not manufactured or distributed by Johnson & Johnson Corporation, owner of the registered trademark Neosporin® Plus Pain Itch Scar.

Inactive Ingredient:

Cocoa Butter, Levant Cottonseed Oil, Olive Oil, Petrolatum, Sodium pyruvate, vitamin E

Questions?

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