NDC 72581-428 Inmotion Pain Creme Ultra Strength

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:
72581-428
Proprietary Name:
Inmotion Pain Creme Ultra Strength
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Inmotion Products Llc
Labeler Code:
72581
Start Marketing Date: [9]
05-12-2019
Listing Expiration Date: [11]
12-31-2020
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
BROWN (C48332)

Product Packages

NDC Code 72581-428-73

Package Description: 1 TUBE in 1 CARTON / 73 mL in 1 TUBE

Product Details

What is NDC 72581-428?

The NDC code 72581-428 is assigned by the FDA to the product Inmotion Pain Creme Ultra Strength which is product labeled by Inmotion Products Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 72581-428-73 1 tube in 1 carton / 73 ml in 1 tube. 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 Inmotion Pain Creme Ultra Strength?

Adults and children over 12 yearsapply generously to affected areamassage painful area until thoroughly absorbed into skinrepeat as necessary up to 3 times daily

Which are Inmotion Pain Creme Ultra Strength UNII Codes?

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

Which are Inmotion Pain Creme Ultra Strength 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".