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  4. NDC Product Code: 22431-134 Petroleum Jelly Baby Fragrance

NDC 22431-134 Petroleum Jelly Baby Fragrance

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 22431-134?
  4. Petroleum Jelly Baby Fragrance 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:
22431-134
Proprietary Name:
Petroleum Jelly Baby Fragrance
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Blue Cross Laboratories, Inc.
Labeler Code:
22431
Product Label ID:
2e758c5b-9add-4567-8c4c-c490e35efce3
Start Marketing Date: [9]
01-25-2019
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 22431-134-01

Package Description: 170 g in 1 JAR

Product Details

What is NDC 22431-134?

The NDC code 22431-134 is assigned by the FDA to the product Petroleum Jelly Baby Fragrance which is product labeled by Blue Cross Laboratories, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 22431-134-01 170 g in 1 jar . 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 Petroleum Jelly Baby Fragrance?

Stop use and ask a doctor if condition worsens or does not improve after 7 days

Which are Petroleum Jelly Baby Fragrance UNII Codes?

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

What is the NDC to RxNorm Crosswalk for Petroleum Jelly Baby Fragrance?

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:

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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".