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  4. NDC Product Code: 59779-877 Cvs Health Multi Symptom Severe Cold Multi Symptom Severe Cold

NDC 59779-877 Cvs Health Multi Symptom Severe Cold Multi Symptom Severe Cold

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 59779-877?
  5. Cvs Health Multi Symptom Severe Cold Multi Symptom Severe Cold 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:
59779-877
Proprietary Name:
Cvs Health Multi Symptom Severe Cold Multi Symptom Severe Cold
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Cvs Pharmacy,inc.
Labeler Code:
59779
Product Label ID:
1dad0528-e99f-45b8-a072-3c6249bf2bcd
Start Marketing Date: [9]
07-21-2015
Listing Expiration Date: [11]
12-31-2020
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Flavor(s):
HONEY (C73394 - GREEN TEA INFUSED WITH HONEY LEMON)

Code Structure Chart

Product Details

What is NDC 59779-877?

The NDC code 59779-877 is assigned by the FDA to the product Cvs Health Multi Symptom Severe Cold Multi Symptom Severe Cold which is product labeled by Cvs Pharmacy,inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 59779-877-06 6 powder, for solution in 1 carton . 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 Cvs Health Multi Symptom Severe Cold Multi Symptom Severe Cold?

•do not use more than directed•take every 4 hours ; not to exceed 6 packets in 24 hours or as directed by a doctorAgeDosechildren under 4 years of agedo not usechildren 4 to under 12 years of agedo not use unless directed by a doctor adults and children 12 years of age and overone packet•dissolve contents of one packet into 8 oz. hot water: sip while hot. Consume entire drink within 10 - 15 minutes.•if using a microwave, add contents of one packet to 8 oz. of cool water: stir briskly before and after heating, Do not overheat.

Which are Cvs Health Multi Symptom Severe Cold Multi Symptom Severe Cold UNII Codes?

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

Which are Cvs Health Multi Symptom Severe Cold Multi Symptom Severe Cold 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 Cvs Health Multi Symptom Severe Cold Multi Symptom Severe Cold?

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".