NDC 78461-0002 Green Remedy Cooling Roll On

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:
78461-0002
Proprietary Name:
Green Remedy Cooling Roll On
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
78461
Start Marketing Date: [9]
03-30-2020
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325 - ROLL ON APPLICATOR)

Code Structure Chart

Product Details

What is NDC 78461-0002?

The NDC code 78461-0002 is assigned by the FDA to the product Green Remedy Cooling Roll On which is product labeled by Exclave Holdings Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 78461-0002-1 1 g in 1 bottle, with applicator . 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 Green Remedy Cooling Roll On?

Temporary relief of minor aches and pains of muscle and joints associated with simple backaches, arthritis, strains, sprains, and bruises.Shake well before use. Apply liberally to affected area. No need to rub in. Repeat if necessary, no more than 4 times daily. Rinse with soap and water to remove. Wash hands with soap and water after use. For children under 12 years of age, consult a physician.

Which are Green Remedy Cooling Roll On UNII Codes?

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

Which are Green Remedy Cooling Roll On 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:

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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".