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  4. NDC Product Code: 73006-108 Only For Cold And Flu Cough Suppressant

NDC 73006-108 Only For Cold And Flu Cough Suppressant

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 73006-108?
  5. Only For Cold And Flu Cough Suppressant 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:
73006-108
Proprietary Name:
Only For Cold And Flu Cough Suppressant
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
O4 Global Trading Usa, Llc
Labeler Code:
73006
Product Label ID:
88edcc93-eb8f-4949-89b3-f398dbee0f10
Start Marketing Date: [9]
02-01-2019
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
ORANGE (C48331)
Shape:
OVAL (C48345)
Size(s):
19 MM
Imprint(s):
S701
Score:
1

Code Structure Chart

Product Details

What is NDC 73006-108?

The NDC code 73006-108 is assigned by the FDA to the product Only For Cold And Flu Cough Suppressant which is product labeled by O4 Global Trading Usa, Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 73006-108-41 1 blister pack in 1 carton / 4 tablet 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 Only For Cold And Flu Cough Suppressant?

Do not take more than directed - See Overdose warningtake with a full glass of water • do not exceed 8 caplets per 24 hours adults and children 12 yrs of age & over2 caplets with water every 4 hrs  children 4 to 12 years of ageask a doctor children under 4 years of agedo not usewhen using other Daytime or Night time products, carefully read each label to ensure correct dosing

Which are Only For Cold And Flu Cough Suppressant UNII Codes?

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

Which are Only For Cold And Flu Cough Suppressant 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 Only For Cold And Flu Cough Suppressant?

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".