Childrens Cold And Cough Day And Night Twin Pack Kit
NDC 49035-925

View dosage, usage, ingredients, routes, and UNII mappings.
Table of Contents
  1. Product Information
  2. Product Packages
  3. What is NDC 49035-925?
  4. Childrens Cold And Cough Day And Night Twin Pack Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes

Product Information

Childrens Cold And Cough Day And Night Twin Pack (onion,matricaria chamomilla,arabica coffee bean,calcium sulfide,goldenseal,sodium chloride,phosphorus,anemone pulsatilla and sulfur) is a UNAPPROVED HOMEOPATHIC-approved product labeled by Wal-mart Stores, Inc. This product is primarily utilized in pharmaceutical processing or compounding. It is supplied as a kit. This product entry covers the primary NDC 49035-925 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.

Primary Identification

NDC Product Code:
49035-925
Proprietary Name:
Childrens Cold And Cough Day And Night Twin Pack
Non-Proprietary Name: [1]
Onion, Matricaria Chamomilla, Arabica Coffee Bean, Calcium Sulfide, Goldenseal, Sodium Chloride, Phosphorus, Anemone Pulsatilla And Sulfur
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Code Navigator:

Clinical Specifications

Dosage Form:
Kit - A packaged collection of related material.

Labeler & Regulatory Data

Labeler Name: [5]
Wal-mart Stores, Inc
Labeler Code:
49035
Product Label ID:
70454f5a-b5ca-8d30-e053-2991aa0a1afc
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.

Marketing Timeline

Start Marketing Date: [9]
07-01-2018
Listing Expiration Date: [11]
12-31-2026
Exclude Flag: [12]
N

Code Structure Chart

Product Details

What is NDC 49035-925?

The NDC code 49035-925 is assigned by the FDA to the product Childrens Cold And Cough Day And Night Twin Pack. It is commonly known by its generic name, onion, matricaria chamomilla, arabica coffee bean, calcium sulfide, goldenseal, sodium chloride, phosphorus, anemone pulsatilla and sulfur. This pharmaceutical product is labeled by Wal-mart Stores, Inc and is currently categorized as listed product. The medication is a kit. In terms of distribution, this product is available in a single package configuration. The associated package NDC(s) include: 49035-925-01. Beyond standard identification, this entry provides technical data including pharmacologic classes, UNII ingredient references, and RxNorm cross-referencing for healthcare systems.

What are the uses of this product?

 Measure only with the dosing cup provided Do not use dosing cup with other products On dosing cup, mL = milliliter, tsp = teaspoonChildren 2 years to under 6 years5mL or 1 teaspoon up to 6 times per day (every 4 hours)Children 6 years to under 12 years10mL or 2 teaspoons up to 6 times per day (every 4 hours)Adults and children 12 years and over15mL or 3 teaspoons up to 6 times per day (every 4 hours)  Measure only with the dosing cup provided Do not use dosing cup with other products On dosing cup, mL = milliliter, tsp = teaspoonChildren 2 years to under 6 years5mL or 1 teaspoon at bedtime and every 4 hours during the night or as necessarChildren 6 years to under 12 years10mL or 2 teaspoons at bedtime and every 4 hours during the night or as necessaryAdults and children 12 years and over15mL or 3 teaspoons at bedtime and every 4 hours during the night or as necessary

Which are the associated UNII Codes?

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

Which are the Inactive Ingredients associated 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 & Regulatory Definitions
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.
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.
What is the Labeler Name? Name of Company corresponding to the labeler code segment of the Product NDC.
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.
What is the Start Marketing Date? This is the date that the labeler indicates was the start of its marketing of the drug product.
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.
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, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".