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  4. NDC Product Code: 22431-706 Baby Soft Scent Petroleum

NDC 22431-706 Baby Soft Scent Petroleum

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 22431-706?
  4. Baby Soft Scent Petroleum 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:
22431-706
Proprietary Name:
Baby Soft Scent Petroleum
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Blue Cross Laboratories, Inc.
Labeler Code:
22431
Product Label ID:
82bd5d2b-a0e4-11d2-e053-2a91aa0a9f96
Start Marketing Date: [9]
02-25-2019
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 22431-706?

The NDC code 22431-706 is assigned by the FDA to the product Baby Soft Scent Petroleum which is product labeled by Blue Cross Laboratories, Inc.. The product's dosage form is . The product is distributed in 5 packages with assigned NDC codes 22431-706-01 113 g in 1 jar , 22431-706-02 170 g in 1 jar , 22431-706-03 226 g in 1 jar , 22431-706-04 270 g in 1 jar , 22431-706-05 368 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 Baby Soft Scent Petroleum?

Useshelps to soothe dry, chapped, cracked or irritated skin and lip due to cold and windfor the temporary protection of minor cuts, scrapes, burns and sunburn

Which are Baby Soft Scent Petroleum UNII Codes?

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

What is the NDC to RxNorm Crosswalk for Baby Soft Scent Petroleum?

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".