NDC 61995-0758 Earths Best Cold Relief Vapor

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:
61995-0758
Proprietary Name:
Earths Best Cold Relief Vapor
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
The Hain Celestial Group, Inc
Labeler Code:
61995
Start Marketing Date: [9]
09-13-2011
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 61995-0758-2

Package Description: 1 JAR in 1 CARTON / 80 g in 1 JAR

Product Details

What is NDC 61995-0758?

The NDC code 61995-0758 is assigned by the FDA to the product Earths Best Cold Relief Vapor which is product labeled by The Hain Celestial Group, Inc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 61995-0758-2 1 jar in 1 carton / 80 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 Earths Best Cold Relief Vapor?

Temporarily relieves cough due to common coldOn muscles and joints, temporarily relieves minor aches and pains

Which are Earths Best Cold Relief Vapor UNII Codes?

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

Which are Earths Best Cold Relief Vapor 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 Earths Best Cold Relief Vapor?

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: 1297310 - camphor 5.3 % / eucalyptus oil 1.3 % / menthol 2.8 % Topical Ointment
  • RxCUI: 1297310 - camphor 0.053 MG/MG / Eucalyptus oil 0.013 MG/MG / menthol 0.028 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".