1. Home
  2. Labeler Index
  3. Cloud 9 Naturally
  4. NDC Product Code: 72070-100 Mercy Pain Relieving

NDC 72070-100 Mercy Pain Relieving

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 72070-100?
  5. Mercy Pain Relieving Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. 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:
72070-100
Proprietary Name:
Mercy Pain Relieving
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Cloud 9 Naturally
Labeler Code:
72070
Product Label ID:
aa584c8f-ab36-474d-af63-49471b900a21
Start Marketing Date: [9]
05-18-2018
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)

Code Structure Chart

Product Details

What is NDC 72070-100?

The NDC code 72070-100 is assigned by the FDA to the product Mercy Pain Relieving which is product labeled by Cloud 9 Naturally. The product's dosage form is . The product is distributed in a single package with assigned NDC code 72070-100-01 113.4 g 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 Mercy Pain Relieving?

• adults and children 2 years of age and older: apply to affected area not more than 3 to 4 times daily. • children under 2 years of age: consult a doctor.

Which are Mercy Pain Relieving UNII Codes?

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

Which are Mercy Pain Relieving 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 Mercy Pain Relieving?

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:

* 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".