1. Home
  2. Labeler Index
  3. Care One (american Sales Company)
  4. NDC Product Code: 41520-473 Daytime Cold And Flu Relief

NDC 41520-473 Daytime Cold And Flu Relief

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 41520-473?
  5. Daytime Cold And Flu Relief 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:
41520-473
Proprietary Name:
Daytime Cold And Flu Relief
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Care One (american Sales Company)
Labeler Code:
41520
Product Label ID:
b2d86c05-ec1a-4676-94e4-82f8be38b281
Start Marketing Date: [9]
11-15-2012
Listing Expiration Date: [11]
12-31-2020
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
ORANGE (C48331)
Shape:
CAPSULE (C48336)
Size(s):
19 MM
Imprint(s):
P19;95A;36A
Score:
1

Code Structure Chart

Product Details

What is NDC 41520-473?

The NDC code 41520-473 is assigned by the FDA to the product Daytime Cold And Flu Relief which is product labeled by Care One (american Sales Company). The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 41520-473-16 2 blister pack in 1 carton / 8 capsule, liquid filled in 1 blister pack, 41520-473-24 2 blister pack in 1 carton / 12 capsule, liquid filled 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 Daytime Cold And Flu Relief?

Take only as directed- see overdose warning do not exceed 4 doses per 24 hours adults and children 12 years and over swallow 2 softgels with water every 4 hours children 4 to under 12 years ask a doctor children under 4 years do not usewhen using other daytime or nitetime products, carefully read each label to insure correct dosing

Which are Daytime Cold And Flu Relief UNII Codes?

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

Which are Daytime Cold And Flu Relief 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 Daytime Cold And Flu Relief?

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: 1086997 - acetaminophen 325 MG / dextromethorphan HBr 10 MG / phenylephrine HCl 5 MG Oral Capsule
  • RxCUI: 1086997 - acetaminophen 325 MG / dextromethorphan hydrobromide 10 MG / phenylephrine hydrochloride 5 MG Oral Capsule
  • RxCUI: 1086997 - APAP 325 MG / dextromethorphan hydrobromide 10 MG / phenylephrine hydrochloride 5 MG Oral Capsule

* 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".