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  4. NDC Product Code: 63736-240 Pronto Plus Pinworm Treatment

NDC 63736-240 Pronto Plus Pinworm Treatment

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 63736-240?
  5. Pronto Plus Pinworm Treatment Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. 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:
63736-240
Proprietary Name:
Pronto Plus Pinworm Treatment
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Insight Pharmaceuticals Llc
Labeler Code:
63736
Product Label ID:
de68a9d1-96c3-4caf-95aa-d034480b9e59
Start Marketing Date: [9]
09-20-2010
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
Flavor(s):
CHERRY (C73375)

Code Structure Chart

Product Details

What is NDC 63736-240?

The NDC code 63736-240 is assigned by the FDA to the product Pronto Plus Pinworm Treatment which is product labeled by Insight Pharmaceuticals Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 63736-240-24 24 carton in 1 case / 1 bottle in 1 carton / 59 ml in 1 bottle. 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 Pronto Plus Pinworm Treatment?

Read package insert carefully before using. Use only according to directions. Do not exceed the recommended dosage unless directed by a doctor.shake well before usingadults and children 2 years of age and older: dose one time as a single dose; do not repeat treatment unless directed by a doctor.find the right dose on chart below. Use weight to dose.use enclosed dosing cup. Do not use with any other device.take any time of day, with or without meals. May be taken alone or with milk or fruit juice. Use of a laxative is not needed before, during, or after taking Pronto Plus.when one individual in a household has pinworms, the entire household should be treated unless otherwise advised. See Warningsif any worms other than pinworms are present before or after treatment, ask a doctorif any symptoms or pinworms are still present after treatment, ask a doctorWeight (lbs)Single Dose (TSP)Under 25 lbs or under 2 yearsAsk a doctor 25-37½38-62163-871 ½88-1122113-1372 ½138-1623163-1873 ½188 and over4

Which are Pronto Plus Pinworm Treatment UNII Codes?

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

Which are Pronto Plus Pinworm Treatment 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 Pronto Plus Pinworm Treatment?

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: 1050119 - Pronto Plus Pinworm 360 MG in 2.5 mL Oral Suspension
  • RxCUI: 1050119 - pyrantel pamoate 144 MG/ML Oral Suspension [Pronto Plus Pinworm]
  • RxCUI: 1050119 - Pronto Plus Pinworm 144 MG/ML (pyrantel base 50 MG/ML) Oral Suspension
  • RxCUI: 1050119 - Pronto Plus Pinworm 360 MG per 2.5 ML (pyrantel base 125 MG per 2.5 ML) Oral Suspension
  • RxCUI: 199106 - pyrantel pamoate 144 MG in 1 mL Oral Suspension

* 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".