NDC 18472-175 Blue Ice Fermented Cod Liver Oil Calm Balm

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
18472-175
Proprietary Name:
Blue Ice Fermented Cod Liver Oil Calm Balm
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Abs Corporation
Labeler Code:
18472
Start Marketing Date: [9]
09-01-2011
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 18472-175-01

Package Description: 49.5 g in 1 JAR

Product Details

What is NDC 18472-175?

The NDC code 18472-175 is assigned by the FDA to the product Blue Ice Fermented Cod Liver Oil Calm Balm which is product labeled by Abs Corporation. The product's dosage form is . The product is distributed in a single package with assigned NDC code 18472-175-01 49.5 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 Blue Ice Fermented Cod Liver Oil Calm Balm?

Directions:Adults and chldren 2 years and over:rub on sore aching musclesnot more than three times per 24 hours or as directed by doctor

Which are Blue Ice Fermented Cod Liver Oil Calm Balm UNII Codes?

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

Which are Blue Ice Fermented Cod Liver Oil Calm Balm 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:

What is the NDC to RxNorm Crosswalk for Blue Ice Fermented Cod Liver Oil Calm Balm?

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: 1492178 - camphor 2.63 % / eucalyptus oil 3.5 % / menthol 0.74 % Topical Ointment
  • RxCUI: 1492178 - camphor 0.0263 MG/MG / Eucalyptus oil 0.035 MG/MG / menthol 0.0074 MG/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".