NDC 55910-139 Dg Health Cold And Allergy

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
55910-139
Proprietary Name:
Dg Health Cold And Allergy
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Dolgencorp Inc
Labeler Code:
55910
Start Marketing Date: [9]
02-26-2010
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
Shape:
ROUND (C48348)
Size(s):
8 MM
Imprint(s):
L358
Score:
2

Product Packages

NDC Code 55910-139-62

Package Description: 1 BLISTER PACK in 1 CARTON / 24 TABLET, FILM COATED in 1 BLISTER PACK

Product Details

What is NDC 55910-139?

The NDC code 55910-139 is assigned by the FDA to the product Dg Health Cold And Allergy which is product labeled by Dolgencorp Inc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 55910-139-62 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 Dg Health Cold And Allergy?

Adults and children 12 years and overtake 1 tablet every 4 to 6 hours do not take more than 6 tablets in 24 hourschildren under 12 yearsdo not use this product in children under 12 years of age

Which are Dg Health Cold And Allergy UNII Codes?

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

What is the NDC to RxNorm Crosswalk for Dg Health Cold And Allergy?

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: 1090443 - chlorpheniramine maleate 4 MG / phenylephrine HCl 10 MG Oral Tablet
  • RxCUI: 1090443 - chlorpheniramine maleate 4 MG / phenylephrine hydrochloride 10 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".