NDC 50066-013 Pomada De La Campana Triple Antibiotic Pain Relief

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
50066-013
Proprietary Name:
Pomada De La Campana Triple Antibiotic Pain Relief
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Genomma Lab Usa, Inc.
Labeler Code:
50066
Start Marketing Date: [9]
06-30-2014
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 50066-013-14

Package Description: 1 TUBE in 1 CARTON / 14 g in 1 TUBE

Product Details

What is NDC 50066-013?

The NDC code 50066-013 is assigned by the FDA to the product Pomada De La Campana Triple Antibiotic Pain Relief which is product labeled by Genomma Lab Usa, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 50066-013-14 1 tube in 1 carton / 14 g in 1 tube. This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Pomada De La Campana Triple Antibiotic Pain Relief?

DirectionsAdults and children 2 years and older:clean affected areaapply a small amount (equal to the surface area of the tip of a finger) on the area 1 to 3 times daily.May be covered with a sterile bandageChildren 2 years and under: ask a doctor

Which are Pomada De La Campana Triple Antibiotic Pain Relief UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Pomada De La Campana Triple Antibiotic Pain Relief Inactive Ingredients UNII Codes?

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. The UNII codes for the inactive ingredients in this product are:

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Product Footnotes

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

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] 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.

[12] 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".