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  4. NDC Product Code: 37012-480 Night Time Cold/flu Relief Multi Symptom

NDC 37012-480 Night Time Cold/flu Relief Multi Symptom

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 37012-480?
  5. Night Time Cold/flu Relief 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:
37012-480
Proprietary Name:
Night Time Cold/flu Relief Multi Symptom
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Shopko Stores Operating Co., Llc.
Labeler Code:
37012
Product Label ID:
d08d5ef8-e0bf-4ef0-9f90-4e30d9828bc3
Start Marketing Date: [9]
08-30-2012
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
GREEN (C48329)
Shape:
CAPSULE (C48336)
Size(s):
20 MM
Imprint(s):
P30;94A;35A
Score:
1

Product Packages

NDC Code 37012-480-20

Package Description: 2 BLISTER PACK in 1 CARTON / 10 CAPSULE, LIQUID FILLED in 1 BLISTER PACK

NDC Code 37012-480-24

Package Description: 2 BLISTER PACK in 1 CARTON / 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK

Product Details

What is NDC 37012-480?

The NDC code 37012-480 is assigned by the FDA to the product Night Time Cold/flu Relief Multi Symptom which is product labeled by Shopko Stores Operating Co., Llc.. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 37012-480-20 2 blister pack in 1 carton / 10 capsule, liquid filled in 1 blister pack, 37012-480-24 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 Night Time Cold/flu Relief Multi Symptom?

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 6 hours children 4 to under 12 years ask a doctor children under 4 years do not usewhen using other Day time or Night time products, carefully read each label to insure correct dosing

Which are Night Time Cold/flu Relief Multi Symptom UNII Codes?

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

Which are Night Time Cold/flu Relief 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 Night Time Cold/flu Relief 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: 1094549 - acetaminophen 325 MG / dextromethorphan HBr 15 MG / doxylamine succinate 6.25 MG Oral Capsule
  • RxCUI: 1094549 - acetaminophen 325 MG / dextromethorphan hydrobromide 15 MG / doxylamine succinate 6.25 MG Oral Capsule
  • RxCUI: 1094549 - APAP 325 MG / dextromethorphan hydrobromide 15 MG / doxylamine succinate 6.25 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".