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  4. NDC Product Code: 10956-618 Pinworm Medicine

NDC 10956-618 Pinworm Medicine

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 10956-618?
  5. Pinworm Medicine Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. NDC to RxNorm Crosswalk
  9. Patient Education

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
10956-618
Proprietary Name:
Pinworm Medicine
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Reese Pharmaceutical Company
Labeler Code:
10956
Product Label ID:
f43e373e-209b-45a0-9102-537c2c3c51f4
Start Marketing Date: [9]
01-01-2007
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Flavor(s):
BANANA (C73364)

Product Packages

NDC Code 10956-618-01

Package Description: 30 mL in 1 BOTTLE, PLASTIC

Product Details

What is NDC 10956-618?

The NDC code 10956-618 is assigned by the FDA to the product Pinworm Medicine which is product labeled by Reese Pharmaceutical Company. The product's dosage form is . The product is distributed in a single package with assigned NDC code 10956-618-01 30 ml 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 Pinworm Medicine?

Uses for the treatment of pinworns

Which are Pinworm Medicine UNII Codes?

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

Which are Pinworm Medicine 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 Pinworm Medicine?

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: 199106 - pyrantel pamoate 144 MG in 1 mL Oral Suspension
  • RxCUI: 199106 - pyrantel pamoate 144 MG/ML Oral Suspension
  • RxCUI: 199106 - pyrantel pamoate 144 MG per 1 ML Oral Suspension
  • RxCUI: 199106 - pyrantel pamoate 144 MG/ML (pyrantel base 50 MG/ML) Oral Suspension

* Please review the disclaimer below.

Patient Education

Pyrantel


Pyrantel, an antiworm medication, is used to treat roundworm, hookworm, pinworm, and other worm infections. This medication is sometimes prescribed for other uses; ask your doctor or pharmacist for more information.
[Learn More]


* 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".