NDC 0363-9998 Childrens Cold And Cough Day And Night Value Pack

Onion,Calcium Sulfide,Sodium Chloride,Anemone Pulsatilla,Arabica Coffee Bean,Matricaria - View Dosage, Usage, Ingredients, Routes, UNII

Product Information

NDC Product Code:
0363-9998
Proprietary Name:
Childrens Cold And Cough Day And Night Value Pack
Non-Proprietary Name: [1]
Onion, Calcium Sulfide, Sodium Chloride, Anemone Pulsatilla, Arabica Coffee Bean, Matricaria Chamomilla, Sulfur, Phosphorus And Goldenseal
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]
Walgreen Company
Labeler Code:
0363
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date: [9]
02-01-2019
Listing Expiration Date: [11]
12-31-2024
Exclude Flag: [12]
N
Code Structure:
Code Navigator:

Product Packages

NDC Code 0363-9998-01

Package Description: 1 KIT in 1 CARTON * 118 mL in 1 BOTTLE, PLASTIC (0363-9997-01) * 118 mL in 1 BOTTLE, PLASTIC (0363-9996-01)

Product Details

What is NDC 0363-9998?

The NDC code 0363-9998 is assigned by the FDA to the product Childrens Cold And Cough Day And Night Value Pack which is a human over the counter drug product labeled by Walgreen Company. The generic name of Childrens Cold And Cough Day And Night Value Pack is onion, calcium sulfide, sodium chloride, anemone pulsatilla, arabica coffee bean, matricaria chamomilla, sulfur, phosphorus and goldenseal. The product's dosage form is kit. The product is distributed in a single package with assigned NDC code 0363-9998-01 1 kit in 1 carton * 118 ml in 1 bottle, plastic (0363-9997-01) * 118 ml in 1 bottle, plastic (0363-9996-01). 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 Childrens Cold And Cough Day And Night Value Pack?

Measure only with the dosing cup providedDo not use dosing cup with other productsOn dosing cup, mL = milliliter, tsp = teaspoonChildren 2 years 5 mLto under 6 years5 mL or 1 teaspoon up to6 times per day (every 4 hours)Children 6 yearsto under 12 years10 mL or 2 teaspoons up to6 times per day (every 4 hours)Adults and children12 years and over15 mL or 3 teaspoons up to6 times per day (every 4 hours) Measure only with the dosing cup providedDo not use dosing cup with other productsOn dosing cup, mL = milliliter, tsp = teaspoonChildren 2 yearsto under 6 years5 mL or 1 teaspoon at bedtimeand every 4 hours duringthe night or as necessaryChildren 6 yearsto under 12 years10 mL or 2 teaspoons atbedtime and every 4 hoursduring the night or as necessaryAdults and children12 years and over15 mL or 3 teaspoons atbedtime and every 4 hoursduring the night or as necessary

Which are Childrens Cold And Cough Day And Night Value Pack UNII Codes?

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

Which are Childrens Cold And Cough Day And Night Value Pack 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:

* Please review the disclaimer below.

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".