NDC 51367-014 Back Pain Relieving Oil

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:
51367-014
Proprietary Name:
Back Pain Relieving Oil
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
International Nature Nutraceuticals
Labeler Code:
51367
Start Marketing Date: [9]
09-01-1966
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 51367-014-40

Package Description: 1 OIL in 1 BOTTLE

Product Details

What is NDC 51367-014?

The NDC code 51367-014 is assigned by the FDA to the product Back Pain Relieving Oil which is product labeled by International Nature Nutraceuticals. The product's dosage form is . The product is distributed in a single package with assigned NDC code 51367-014-40 1 oil in 1 bottle . 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 Back Pain Relieving Oil?

Adults and children 6 years of age and older: Apply toaffected area not more than 3~4 times daily. Childrenunder 6 years of age: Do not use, consult a doctor.成人及六歲以上的兒童, 塗在患處緩和地旋轉直至完全滲透,每日3-4次. 六歲以下的小童請諮詢醫生.

Which are Back Pain Relieving Oil UNII Codes?

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

Which are Back Pain Relieving Oil 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 Back Pain Relieving Oil?

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: 1441310 - camphor 9 % / menthol 11 % / methyl salicylate 17 % Topical Oil
  • RxCUI: 1441310 - camphor 90 MG/ML / menthol 110 MG/ML / methyl salicylate 170 MG/ML Topical Oil

* 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".