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  4. NDC Product Code: 64525-0603 Family Dollar Multi-symptom Severe Cold Green Tea And Honey Lemon Flavors

NDC 64525-0603 Family Dollar Multi-symptom Severe Cold Green Tea And Honey Lemon Flavors

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 64525-0603?
  5. Family Dollar Multi-symptom Severe Cold Green Tea And Honey Lemon Flavors 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:
64525-0603
Proprietary Name:
Family Dollar Multi-symptom Severe Cold Green Tea And Honey Lemon Flavors
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Quality Home Products
Labeler Code:
64525
Product Label ID:
253d4156-55e9-4d3f-e054-00144ff88e88
Start Marketing Date: [9]
11-23-2015
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
YELLOW (C48330 - CARAMEL COLOR)
YELLOW (C48330 - D AND C YELLOW NO. 10)
Flavor(s):
HONEY (C73394 - NATURAL HONEY AND LEMON FLAVOR)
LEMON (C73396 - NATURAL HONEY AND LEMON FLAVOR)

Code Structure Chart

Product Details

What is NDC 64525-0603?

The NDC code 64525-0603 is assigned by the FDA to the product Family Dollar Multi-symptom Severe Cold Green Tea And Honey Lemon Flavors which is product labeled by Quality Home Products. The product's dosage form is . The product is distributed in a single package with assigned NDC code 64525-0603-6 6 granule, for solution in 1 box . 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 Family Dollar Multi-symptom Severe Cold Green Tea And Honey Lemon Flavors?

When using this product - do not exceed recommended dosage.

Which are Family Dollar Multi-symptom Severe Cold Green Tea And Honey Lemon Flavors UNII Codes?

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

Which are Family Dollar Multi-symptom Severe Cold Green Tea And Honey Lemon Flavors 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 Family Dollar Multi-symptom Severe Cold Green Tea And Honey Lemon Flavors?

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: 1189316 - acetaminophen 500 MG / dextromethorphan HBr 20 MG / phenylephrine HCl 10 MG Granules for Oral Solution
  • RxCUI: 1189316 - acetaminophen 500 MG / dextromethorphan hydrobromide 20 MG / phenylephrine hydrochloride 10 MG Granules for Oral Solution
  • RxCUI: 1189316 - acetaminophen 500 MG / dextromethorphan HBr 20 MG / phenylephrine HCl 10 MG Packet for Oral Solution
  • RxCUI: 1189316 - acetaminophen 500 MG / dextromethorphan hydrobromide 20 MG / phenylephrine hydrochloride 10 MG Powder for Oral Solution
  • RxCUI: 1189316 - APAP 500 MG / Dextromethorphan Hydrobromide 20 MG / Phenylephrine Hydrochloride 10 MG Granules for Oral Solution

* 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".