NDC 50145-222 Hipoglos

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:
50145-222
Proprietary Name:
Hipoglos
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Laboratorios Andromaco S.a.
Labeler Code:
50145
Start Marketing Date: [9]
11-03-2010
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Packages

NDC Code 50145-222-01

Package Description: 1 TUBE in 1 CARTON / 120 g in 1 TUBE

NDC Code 50145-222-02

Package Description: 1 TUBE in 1 CARTON / 100 g in 1 TUBE

NDC Code 50145-222-03

Package Description: 1 TUBE in 1 CARTON / 72 g in 1 TUBE

NDC Code 50145-222-04

Package Description: 1 TUBE in 1 CARTON / 60 g in 1 TUBE

NDC Code 50145-222-05

Package Description: 1 TUBE in 1 CARTON / 5 g in 1 TUBE

Product Details

What is NDC 50145-222?

The NDC code 50145-222 is assigned by the FDA to the product Hipoglos which is product labeled by Laboratorios Andromaco S.a.. The product's dosage form is . The product is distributed in 5 packages with assigned NDC codes 50145-222-01 1 tube in 1 carton / 120 g in 1 tube, 50145-222-02 1 tube in 1 carton / 100 g in 1 tube, 50145-222-03 1 tube in 1 carton / 72 g in 1 tube, 50145-222-04 1 tube in 1 carton / 60 g in 1 tube, 50145-222-05 1 tube in 1 carton / 5 g 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 Hipoglos?

Change wet or soiled diapers promptly.Clean the diaper area.Allow to dry.Apply ointment liberally as often as necessary, with each diaper change, especially at bedtime or any time when exposure to wet diapers may be prolonged.

Which are Hipoglos UNII Codes?

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

Which are Hipoglos 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 Hipoglos?

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: 1249131 - lanolin 15 % / zinc oxide 15 % Topical Ointment
  • RxCUI: 1249131 - lanolin 0.15 MG/MG / zinc oxide 0.15 MG/MG Topical Ointment
  • RxCUI: 1249131 - Lanolin 0.15 MG/MG / ZNO 0.15 MG/MG Topical Ointment

* 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".