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  4. NDC Product Code: 72886-3022 Crystal Chest Rub

NDC 72886-3022 Crystal Chest Rub

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 72886-3022?
  4. Crystal Chest Rub Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes
  7. 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:
72886-3022
Proprietary Name:
Crystal Chest Rub
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Crystal Curam
Labeler Code:
72886
Product Label ID:
87b30973-5367-8d4d-e053-2995a90ab56b
Start Marketing Date: [9]
04-09-2019
Listing Expiration Date: [11]
12-31-2020
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 72886-3022-1

Package Description: 113 g in 1 JAR

Product Details

What is NDC 72886-3022?

The NDC code 72886-3022 is assigned by the FDA to the product Crystal Chest Rub which is product labeled by Crystal Curam. The product's dosage form is . The product is distributed in a single package with assigned NDC code 72886-3022-1 113 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 Crystal Chest Rub?

See important warnings under " When using this product" adults and children 2 years and overrub a thick layer on throat & chest &cover with a warm, dry cloth if desiredkeep clothing loose about throat and chest to help vapors reach the nose and mouthuse up to three times daily or as directed by doctorfor muscle/joint minor aches and pains apply to affected area not more than 3 to 4 times dailychildren under 2 years: do not use

Which are Crystal Chest Rub UNII Codes?

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

Which are Crystal Chest Rub 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 Crystal Chest Rub?

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: 2166605 - camphor 4.8 % / eucalyptus oil 2.6 % / menthol 1.2 % Topical Ointment
  • RxCUI: 2166605 - camphor 0.048 MG/MG / Eucalyptus oil 0.026 MG/MG / menthol 0.012 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".