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  4. NDC Product Code: 59779-583 Allergy And Cold

NDC 59779-583 Allergy And Cold

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 59779-583?
  5. Allergy And Cold Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
59779-583
Proprietary Name:
Allergy And Cold
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Woonsocket Prescription Center,incorporated
Labeler Code:
59779
Product Label ID:
f09755f7-667b-4441-a6d6-c7f709f286df
Start Marketing Date: [9]
07-10-2009
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
YELLOW (C48330 - PINK WITH GREY BAND)
Shape:
CAPSULE (C48336)
Size(s):
19 MM
Imprint(s):
L;3
Score:
1

Product Packages

NDC Code 59779-583-08

Package Description: 1 BLISTER PACK in 1 CARTON / 24 CAPSULE, GELATIN COATED in 1 BLISTER PACK

Product Details

What is NDC 59779-583?

The NDC code 59779-583 is assigned by the FDA to the product Allergy And Cold which is product labeled by Woonsocket Prescription Center,incorporated. The product's dosage form is . The product is distributed in a single package with assigned NDC code 59779-583-08 1 blister pack in 1 carton / 24 capsule, gelatin 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 Allergy And Cold?

Do not use more than directed (see overdose warning)adults and children 12 years and overtake 2 gelcaps every 4 hoursdo not take more than 12 gelcaps in 24 hourschildren under 12 yearsdo not use this adult product in children under 12 years of age; this will provide more than the recommended dose (overdose) and may cause liver damage

Which are Allergy And Cold UNII Codes?

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

Which are Allergy And Cold 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:

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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".