NDC 72004-001 Strong Vaporizing

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:
72004-001
Proprietary Name:
Strong Vaporizing
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Afn Broker Llc.
Labeler Code:
72004
Start Marketing Date: [9]
07-01-2018
Listing Expiration Date: [11]
12-31-2020
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Size(s):
150 MM

Product Packages

NDC Code 72004-001-04

Package Description: 113 g in 1 JAR

Product Details

What is NDC 72004-001?

The NDC code 72004-001 is assigned by the FDA to the product Strong Vaporizing which is product labeled by Afn Broker Llc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 72004-001-04 113 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 Strong Vaporizing?

SEE IMPORTANT WARMING UNDER "WHEN USING THIS PRODUCT" *ADULTS AND CHILDREN 2 YEARS AND OVER*RUB A THICK LAYER ON CHEST & THROAT OR RUB ON SORE ACHING MUSCLES*COVER WITH A WARM DRY CLOTH IF DESIRED*KEEP CLOTHING LOOSE ABOUT THROAT/CHEST TO HELP VAPORS REACH NOSE/MOUTH*REPEAT UP TO THREE TIMES PER 24 HOUSES OR AS DIRECTED BY A DOCTOR*CHILDREN UNDER 2 YEARS OF AGE: ASK A DOCTOR

Which are Strong Vaporizing UNII Codes?

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

Which are Strong Vaporizing 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 Strong Vaporizing?

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: 1099014 - camphor 5.25 % / eucalyptus oil 1.6 % / menthol 3.15 % Topical Ointment
  • RxCUI: 1099014 - camphor 0.0525 MG/MG / Eucalyptus oil 0.016 MG/MG / menthol 0.0315 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".