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  4. NDC Product Code: 49348-834 Medicated Body

NDC 49348-834 Medicated Body

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 49348-834?
  4. Medicated Body Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes
  7. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
49348-834
Proprietary Name:
Medicated Body
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Mckesson
Labeler Code:
49348
Product Label ID:
487fd9a6-1e96-4af3-9433-ebdb6bce6b89
Start Marketing Date: [9]
06-18-1994
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 49348-834-92

Package Description: .283 kg in 1 BOTTLE, PLASTIC

Price per Unit: $0.01042 per GM

Product Details

What is NDC 49348-834?

The NDC code 49348-834 is assigned by the FDA to the product Medicated Body which is product labeled by Mckesson. The product's dosage form is . The product is distributed in a single package with assigned NDC code 49348-834-92 .283 kg in 1 bottle, plastic . 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 Medicated Body?

Uses for temporary relief of pain and itching due to:•minor cuts      •sunburn           •insect bites•poison ivy       •poison oak      •poison sumac•scrapes            •minor burns    •minor skin irritationsdries the oozing and weeping of:•poison ivy       •poison oak      •poison sumac

Which are Medicated Body UNII Codes?

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

Which are Medicated Body 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 Medicated Body?

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: 577232 - menthol 0.15 % / zinc oxide 1 % Topical Powder
  • RxCUI: 577232 - menthol 0.0015 MG/MG / zinc oxide 0.01 MG/MG Topical Powder
  • RxCUI: 577232 - Menthol 0.0015 MG/MG / ZNO 0.01 MG/MG Topical Powder

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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".