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  4. NDC Product Code: 82199-530 Triple Antibiotic

NDC 82199-530 Triple Antibiotic

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 82199-530?
  4. Triple Antibiotic Uses
  5. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
82199-530
Proprietary Name:
Triple Antibiotic
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Shandong Ruian Pharmaceutical Co.,ltd.
Labeler Code:
82199
Product Label ID:
cae7322c-17de-0d81-e053-2a95a90a08d7
Start Marketing Date: [9]
08-26-2021
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
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Product Details

What is NDC 82199-530?

The NDC code 82199-530 is assigned by the FDA to the product Triple Antibiotic which is product labeled by Shandong Ruian Pharmaceutical Co.,ltd.. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 82199-530-11 14.2 g in 1 tube , 82199-530-12 28.3 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 Triple Antibiotic?

First aid to help prevent infection and for temporary relief of pain or discomfort in minor: • cuts • scrapes • burns

What is the NDC to RxNorm Crosswalk for Triple Antibiotic?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:
  • RxCUI: 2281302 - bacitracin 500 UNT / lidocaine HCl 40 MG / neomycin 3.5 MG / polymyxin B 5,000 UNT per GM Topical Ointment
  • RxCUI: 2281302 - bacitracin 0.5 UNT/MG / lidocaine hydrochloride 0.04 MG/MG / neomycin 0.0035 MG/MG / polymyxin B 5 UNT/MG Topical Ointment

* Please review the disclaimer below.

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".