NDC 51681-0011 White Flower Analgesic Balm Floral Scented

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:
51681-0011
Proprietary Name:
White Flower Analgesic Balm Floral Scented
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Jelma Philippines Inc
Labeler Code:
51681
Start Marketing Date: [9]
07-20-2010
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 51681-0011-1

Package Description: 10 mL in 1 BOTTLE, GLASS

NDC Code 51681-0011-2

Package Description: 5 mL in 1 BOTTLE, GLASS

Product Details

What is NDC 51681-0011?

The NDC code 51681-0011 is assigned by the FDA to the product White Flower Analgesic Balm Floral Scented which is product labeled by Jelma Philippines Inc. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 51681-0011-1 10 ml in 1 bottle, glass , 51681-0011-2 5 ml in 1 bottle, glass . 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 White Flower Analgesic Balm Floral Scented?

This product is used as PurposeExternal analgesicUses For the temporary relief of minor aches and pains of muscles and joints due to:simple backachearthritisstrainsbruisessprains

Which are White Flower Analgesic Balm Floral Scented UNII Codes?

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

What is the NDC to RxNorm Crosswalk for White Flower Analgesic Balm Floral Scented?

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: 1053359 - camphor 5.4 % / menthol 13.1 % / methyl salicylate 36 % Topical Oil
  • RxCUI: 1053359 - camphor 54 MG/ML / menthol 131 MG/ML / methyl salicylate 360 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".