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  4. NDC Product Code: 59779-526 Severe Cold Relief Pe

NDC 59779-526 Severe Cold Relief Pe

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 59779-526?
  5. Severe Cold Relief Pe 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:
59779-526
Proprietary Name:
Severe Cold Relief Pe
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Woonsocket Prescription Center, Incorporated
Labeler Code:
59779
Product Label ID:
5a251962-305d-101b-e7fa-cb6b50c20a4f
Start Marketing Date: [9]
06-21-2005
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
Shape:
CAPSULE (C48336)
Size(s):
17 MM
Imprint(s):
44;526
Score:
1

Code Structure Chart

Product Details

What is NDC 59779-526?

The NDC code 59779-526 is assigned by the FDA to the product Severe Cold Relief Pe which is product labeled by Woonsocket Prescription Center, Incorporated. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 59779-526-02 1 blister pack in 1 carton / 12 tablet, film coated in 1 blister pack, 59779-526-08 1 blister pack in 1 carton / 24 tablet, film coated in 1 blister pack. 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 Severe Cold Relief Pe?

Do not use more than directed (see overdose warning)adults and children 12 years and overtake 2 caplets every 4 hoursdo not take more than 12 caplets in 24 hourschildren 6 to under 12 years of agetake one caplet every 4 hoursdo not take more than 5 caplets in 24 hourschildren under 6 years of agedo not use this product in children under 6 years of age; this will provide more than the recommended dose (overdose) and may cause liver damage

Which are Severe Cold Relief Pe UNII Codes?

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

Which are Severe Cold Relief Pe 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 Severe Cold Relief Pe?

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: 1233575 - acetaminophen 325 MG / diphenhydrAMINE HCl 12.5 MG / phenylephrine HCl 5 MG Oral Tablet
  • RxCUI: 1233575 - acetaminophen 325 MG / diphenhydramine hydrochloride 12.5 MG / phenylephrine hydrochloride 5 MG Oral Tablet
  • RxCUI: 1233575 - acetaminophen 325 MG / diphenhydramine HCl 12.5 MG / phenylephrine HCl 5 MG Oral Tablet
  • RxCUI: 1233575 - APAP 325 MG / Diphenhydramine Hydrochloride 12.5 MG / Phenylephrine Hydrochloride 5 MG Oral Tablet

* 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".