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  4. NDC Product Code: 71391-125 Cmc Pain Relieving

NDC 71391-125 Cmc Pain Relieving

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 71391-125?
  4. Cmc Pain Relieving Uses
  5. Active Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
71391-125
Proprietary Name:
Cmc Pain Relieving
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Unexo Life Sciences, Private Limited
Labeler Code:
71391
Product Label ID:
4bf629d1-f43a-4496-8ff5-79df53d18235
Start Marketing Date: [9]
06-01-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 71391-125?

The NDC code 71391-125 is assigned by the FDA to the product Cmc Pain Relieving which is product labeled by Unexo Life Sciences, Private Limited. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 71391-125-01 1 patch in 1 pouch , 71391-125-06 6 pouch in 1 box / 1 patch in 1 pouch. 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 Cmc Pain Relieving?

Adults and children 12 years of age and older: apply to the affected area not more than 3 to 4 times dailyChildren under 12 years of age consult a doctorclean and dry affected arearemove patch from filmapply sticky side of patch to affected area use one patch at a timeleave patch on affected area for up to 8 hours at a time

Which are Cmc Pain Relieving UNII Codes?

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

  • .ALPHA.,.ALPHA.-DIBROMO-D-CAMPHOR (UNII: F89Z8SAG3O)
  • .ALPHA.,.ALPHA.-DIBROMO-D-CAMPHOR (UNII: F89Z8SAG3O) (Active Moiety)
  • MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)
  • MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (Active Moiety)
  • CAPSAICIN (UNII: S07O44R1ZM)
  • CAPSAICIN (UNII: S07O44R1ZM) (Active Moiety)

* 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".