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NDC 0363-7872 Walgreens Maximum Strength Triple Antibiotic With Pain Relief

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 0363-7872?
  4. Walgreens Maximum Strength Triple Antibiotic With Pain Relief Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
0363-7872
Proprietary Name:
Walgreens Maximum Strength Triple Antibiotic With Pain Relief
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Walgreen Co.
Labeler Code:
0363
Product Label ID:
1aef7104-94d9-436f-890b-d8371ba34aaf
Start Marketing Date: [9]
05-13-2015
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
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Product Details

What is NDC 0363-7872?

The NDC code 0363-7872 is assigned by the FDA to the product Walgreens Maximum Strength Triple Antibiotic With Pain Relief which is product labeled by Walgreen Co.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 0363-7872-28 1 tube in 1 carton / 28 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 Walgreens Maximum Strength Triple Antibiotic With Pain Relief?

Directionsadults and children 2 years of age 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 of age: ask a doctor

Which are Walgreens Maximum Strength Triple Antibiotic With Pain Relief UNII Codes?

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

Which are Walgreens Maximum Strength Triple Antibiotic With 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".