NDC 55758-046 Parche Leon Milagroso Dual Action

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory .
NDC Product Code:
55758-046
Proprietary Name:
Parche Leon Milagroso Dual Action
Product Type: [3]
Labeler Name: [5]
Labeler Code:
55758
Start Marketing Date: [9]
02-01-2016
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
U
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Product Details

What is NDC 55758-046?

The NDC code 55758-046 is assigned by the FDA to the product Parche Leon Milagroso Dual Action which is product labeled by Pharmadel Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 55758-046-06 6 pouch in 1 carton / 2.27 g in 1 pouch. 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 Parche Leon Milagroso Dual Action?

Adults & children 12 yrs of age & older: apply to affected area not more than 3 to 4 times daily children under 2 year of age: consult a doctor clean and dry affected arearemove patch from filmapply sticky side of patch to affected areause one patch at a timeleave patch on affected area for up to 8-hours at a time

Which are Parche Leon Milagroso Dual Action UNII Codes?

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

Which are Parche Leon Milagroso Dual Action 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 Parche Leon Milagroso Dual Action?

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: 1300889 - capsaicin 0.0375 % / menthol 5 % Medicated Patch
  • RxCUI: 1300889 - capsaicin 0.000375 MG/MG / menthol 0.05 MG/MG Medicated Patch

* 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".