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NDC 71971-6155 Real Relief Natural Wellness Cough And Cold Syrup Combo Pack Daytime Formula And Nighttime Formula

Drosera Rotundifolia Flowering Top,Arnica Montana,Bryonia Alba Whole,Ipecacuanha - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 71971-6155?
  4. Real Relief Natural Wellness Cough And Cold Syrup Combo Pack Daytime Formula And Nighttime Formula Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes

Product Information

NDC Product Code:
71971-6155
Proprietary Name:
Real Relief Natural Wellness Cough And Cold Syrup Combo Pack Daytime Formula And Nighttime Formula
Non-Proprietary Name: [1]
Drosera Rotundifolia Flowering Top, Arnica Montana, Bryonia Alba Whole, Ipecacuanha (ipecac), Cetraria Islandica Subsp. Islandica, Cochineal (coccus Cacti), Corallium Rubrum Whole, Stannum Metallicum (tin), Chamomilla (german Chamomille), Coffea Cruda (coffee)
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Kit - A packaged collection of related material.
Labeler Name: [5]
Homeolab International (canada) Inc
Labeler Code:
71971
Product Label ID:
b97993b4-54ab-41af-b385-227a25e64c6b
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date: [9]
09-01-2022
Listing Expiration Date: [11]
12-31-2024
Exclude Flag: [12]
N
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Product Details

What is NDC 71971-6155?

The NDC code 71971-6155 is assigned by the FDA to the product Real Relief Natural Wellness Cough And Cold Syrup Combo Pack Daytime Formula And Nighttime Formula which is a human over the counter drug product labeled by Homeolab International (canada) Inc. The generic name of Real Relief Natural Wellness Cough And Cold Syrup Combo Pack Daytime Formula And Nighttime Formula is drosera rotundifolia flowering top, arnica montana, bryonia alba whole, ipecacuanha (ipecac), cetraria islandica subsp. islandica, cochineal (coccus cacti), corallium rubrum whole, stannum metallicum (tin), chamomilla (german chamomille), coffea cruda (coffee). The product's dosage form is kit. The product is distributed in a single package with assigned NDC code 71971-6155-7 1 kit in 1 kit * 1 bottle in 1 carton (71971-9204-5) / 100 ml in 1 bottle * 1 bottle in 1 carton (71971-9185-5) / 100 ml in 1 bottle. 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 Real Relief Natural Wellness Cough And Cold Syrup Combo Pack Daytime Formula And Nighttime Formula?

Part 1 Real Relief Natural Wellness™ Daytime SyrupDirections: • Do not exceed recommended dosage • Do not take with foods • Repeat every 4 hours and reduce with improvement or as directed by a health professional. Age………………………………………………………….Dose Adults and Children 12 + years. ...........10 ml or 2 teaspoon (tsp) Children 6 to 11 years of age. ...............5 ml or 1 teaspoon (tsp) Children 2 to 5 years of age. .................2.5 ml or ½ teaspoon (tsp) Part 2 Real Relief Natural Wellness™ Relief Nighttime SyrupDirections: • Do not exceed recommended dosage • Do not take with foods • Repeat every 8 hours and reduce with improvement or as directed by a health professional. Age………………………………………………………….Dose Adults and Children 12 + years. ............10 ml or 2 teaspoon (tsp) Children 6 to 11 years of age. ................5 ml or 1 teaspoon (tsp) Children 2 to 5 years of age. ..................2.5 ml or ½ teaspoon (tsp)

Which are Real Relief Natural Wellness Cough And Cold Syrup Combo Pack Daytime Formula And Nighttime Formula UNII Codes?

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

Which are Real Relief Natural Wellness Cough And Cold Syrup Combo Pack Daytime Formula And Nighttime Formula 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:

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Product Footnotes

[1] What is the Non-Proprietary Name? - The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

[3] What kind of product is this? - Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

[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".