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  4. NDC Product Code: 24385-066 Good Neighbor Pharmacy Cold Multi Symptom

NDC 24385-066 Good Neighbor Pharmacy Cold Multi Symptom

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 24385-066?
  5. Good Neighbor Pharmacy Cold Multi Symptom 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:
24385-066
Proprietary Name:
Good Neighbor Pharmacy Cold Multi Symptom
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Amerisource Bergen
Labeler Code:
24385
Product Label ID:
34de34ae-1036-4652-bc3d-b922dc5a283e
Start Marketing Date: [9]
03-30-1993
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
YELLOW (C48330)
Shape:
OVAL (C48345)
Size(s):
20 MM
Imprint(s):
L234
Score:
1
Flavor(s):
VANILLA (C73421 - MENTHOL)

Product Packages

NDC Code 24385-066-62

Package Description: 2 BLISTER PACK in 1 CARTON / 12 TABLET, FILM COATED in 1 BLISTER PACK

Price per Unit: $0.09409 per EA

Product Details

What is NDC 24385-066?

The NDC code 24385-066 is assigned by the FDA to the product Good Neighbor Pharmacy Cold Multi Symptom which is product labeled by Amerisource Bergen. The product's dosage form is . The product is distributed in a single package with assigned NDC code 24385-066-62 2 blister pack in 1 carton / 12 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 Good Neighbor Pharmacy Cold Multi Symptom?

Do not take more than directed (see Liver warning)adults and children 12 years and overtake 2 caplets every 4 hoursswallow whole – do not crush, chew or dissolvedo not take more than 12 caplets in 24 hourschildren under 12 yearsdo not use this adult product in children under 12 years of age

Which are Good Neighbor Pharmacy Cold Multi Symptom UNII Codes?

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

Which are Good Neighbor Pharmacy Cold Multi Symptom 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 Good Neighbor Pharmacy Cold Multi Symptom?

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: 1110988 - acetaminophen 325 MG / dextromethorphan HBr 10 MG / guaiFENesin 200 MG / phenylephrine HCl 5 MG Oral Tablet
  • RxCUI: 1110988 - acetaminophen 325 MG / dextromethorphan hydrobromide 10 MG / guaifenesin 200 MG / phenylephrine hydrochloride 5 MG Oral Tablet
  • RxCUI: 1110988 - APAP 325 MG / dextromethorphan hydrobromide 10 MG / guaifenesin 200 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".