NDC 52564-308 Hot Stuff

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:
52564-308
Proprietary Name:
Hot Stuff
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Mueller Sports Medicine Llc
Labeler Code:
52564
Start Marketing Date: [9]
06-25-2014
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 52564-308-02

Package Description: 106 g in 1 BOTTLE, PUMP

Product Details

What is NDC 52564-308?

The NDC code 52564-308 is assigned by the FDA to the product Hot Stuff which is product labeled by Mueller Sports Medicine Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 52564-308-02 106 g in 1 bottle, pump . 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 Hot Stuff?

Rotate pump's spout counter-clockwise slightly to unlock; clockwise to lockChildren under 12 years of age consult a physicianApply a thin layer to affected area not more than 3 to 4 times dailyGently massage into the skin until fully absorbedWash hands with soap and water after each application to avoid spreading to the eyes or other sensitive mucous membranesA burning sensation may occur upon initial application but generally disappears with continued useFor a severe burning discomfort, remove excess product wiht a soft cloth and mineral oil

Which are Hot Stuff UNII Codes?

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

Which are Hot Stuff 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 Hot Stuff?

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".