NDC 33346-3401 Mobility

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:
33346-3401
Proprietary Name:
Mobility
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Mayway Corporation
Labeler Code:
33346
Start Marketing Date: [9]
10-26-2018
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 33346-3401-2

Package Description: 1 VIAL, GLASS in 1 BOX / 50 mL in 1 VIAL, GLASS (33346-3401-1)

Product Details

What is NDC 33346-3401?

The NDC code 33346-3401 is assigned by the FDA to the product Mobility which is product labeled by Mayway Corporation. The product's dosage form is . The product is distributed in a single package with assigned NDC code 33346-3401-2 1 vial, glass in 1 box / 50 ml in 1 vial, glass (33346-3401-1). 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 Mobility?

Pregnant or breastfeeding women and children under 12: Do not use or consult a doctor adults and children 12 years of age and older: Apply generously to the affected area and massage until thoroughly absorbed into skinrepeat as necessary but not more than 4 times daily.pregnant or breastfeeding women and children under 3: Do not use or consult a doctor

Which are Mobility UNII Codes?

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

Which are Mobility 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 Mobility?

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: 2101502 - camphor oil 4 % / Capsicum oleoresin 0.25 % / menthol 8 % / methyl salicylate 20 % Topical Oil
  • RxCUI: 2101502 - camphor oil 40 MG/ML / Capsicum oleoresin 2.5 MG/ML / menthol 80 MG/ML / methyl salicylate 200 MG/ML Topical Oil

* 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".