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  4. NDC Product Code: 42947-630 Obstetrical Antiseptic

NDC 42947-630 Obstetrical Antiseptic

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 42947-630?
  4. Obstetrical Antiseptic Uses
  5. Active Ingredients UNII Codes
  6. 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:
42947-630
Proprietary Name:
Obstetrical Antiseptic
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Wuxi Medical Instrument Factory
Labeler Code:
42947
Product Label ID:
4ee8955d-9e82-46fd-88c5-b45196145285
Start Marketing Date: [9]
01-01-2009
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
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Product Details

What is NDC 42947-630?

The NDC code 42947-630 is assigned by the FDA to the product Obstetrical Antiseptic which is product labeled by Wuxi Medical Instrument Factory. The product's dosage form is . The product is distributed in a single package with assigned NDC code 42947-630-03 1.4 ml in 1 pouch . 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 Obstetrical Antiseptic?

Directions* Clean the affected area* Apply a small amount of this product on the area 1 to 3 times daily* May be covered with a sterile bandage when dry

Which are Obstetrical Antiseptic UNII Codes?

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

What is the NDC to RxNorm Crosswalk for Obstetrical Antiseptic?

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:

* 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".