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  4. NDC Product Code: 70692-103 Multi Symptom Sinus Relief Pain And Congestion Daytime Nighttime

NDC 70692-103 Multi Symptom Sinus Relief Pain And Congestion Daytime Nighttime

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 70692-103?
  5. Multi Symptom Sinus Relief Pain And Congestion Daytime Nighttime 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:
70692-103
Proprietary Name:
Multi Symptom Sinus Relief Pain And Congestion Daytime Nighttime
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Strive Pharmaceuticals Inc.
Labeler Code:
70692
Product Label ID:
67dcb6fa-c14b-8413-e053-2991aa0a4ace
Start Marketing Date: [9]
03-01-2018
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
ORANGE (C48331 - REDDISH ORANGE)
BLUE (C48333)
Shape:
OVAL (C48345)
Size(s):
19 MM
Imprint(s):
S703
S704
Score:
1

Code Structure Chart

Product Details

What is NDC 70692-103?

The NDC code 70692-103 is assigned by the FDA to the product Multi Symptom Sinus Relief Pain And Congestion Daytime Nighttime which is product labeled by Strive Pharmaceuticals Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 70692-103-12 1 kit in 1 package, combination * 8 tablet, film coated in 1 blister pack * 4 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 Multi Symptom Sinus Relief Pain And Congestion Daytime Nighttime?

* temporarily relieves:nasal congestionheadacheminor aches and painsinus congestion and pressurerunny nose and sneezing (Nighttime only)cough (Nighttime only)* temporarily promotes nasal and/or sinus drainag* helps loosen phlegm (mucus) and thin bronchial secretions to rid the bronchial passageways of bothersome mucus and make coughs more productive (Daytime only)

Which are Multi Symptom Sinus Relief Pain And Congestion Daytime Nighttime UNII Codes?

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

Which are Multi Symptom Sinus Relief Pain And Congestion Daytime Nighttime 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 Multi Symptom Sinus Relief Pain And Congestion Daytime Nighttime?

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: 1233575 - acetaminophen 325 MG / diphenhydrAMINE HCl 12.5 MG / phenylephrine HCl 5 MG Oral Tablet
  • RxCUI: 1233575 - acetaminophen 325 MG / diphenhydramine hydrochloride 12.5 MG / phenylephrine hydrochloride 5 MG Oral Tablet
  • RxCUI: 1233575 - acetaminophen 325 MG / diphenhydramine HCl 12.5 MG / phenylephrine HCl 5 MG Oral Tablet
  • RxCUI: 1233575 - APAP 325 MG / Diphenhydramine Hydrochloride 12.5 MG / Phenylephrine Hydrochloride 5 MG Oral Tablet
  • RxCUI: 1243679 - acetaminophen 325 MG / guaiFENesin 200 MG / phenylephrine HCl 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".