NDC 69851-102 Therapeutic Icy Cold Cooling Pain Relief

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:
69851-102
Proprietary Name:
Therapeutic Icy Cold Cooling Pain Relief
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Apex-carex Heathcare Products
Labeler Code:
69851
Start Marketing Date: [9]
05-15-2015
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 69851-102-24

Package Description: 118 mL in 1 BOTTLE, SPRAY

Product Details

What is NDC 69851-102?

The NDC code 69851-102 is assigned by the FDA to the product Therapeutic Icy Cold Cooling Pain Relief which is product labeled by Apex-carex Heathcare Products. The product's dosage form is . The product is distributed in a single package with assigned NDC code 69851-102-24 118 ml in 1 bottle, spray . 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 Therapeutic Icy Cold Cooling Pain Relief?

SHAKE GENTLYADULTS AND CHILDREN 2 YEARS OF AGE AND OLDER, SPRAY ONTO AFFECTED AREA NOT MORE THAN 3 TO 4 TIMES DAILY.RUB IN THOROUGHLY UNTIL GEL IS ABSORBED.

Which are Therapeutic Icy Cold Cooling Pain Relief UNII Codes?

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

Which are Therapeutic Icy Cold Cooling Pain Relief 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 Therapeutic Icy Cold Cooling Pain Relief?

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:

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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".