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
- 0363 - Walgreen Company
- 0363-9998 - Childrens Cold And Cough Day And Night Value Pack
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?
What are the uses for Childrens Cold And Cough Day And Night Value Pack?
Which are Childrens Cold And Cough Day And Night Value Pack UNII Codes?
The UNII codes for the active ingredients in this product are:
- ARABICA COFFEE BEAN (UNII: 3SW678MX72)
- ARABICA COFFEE BEAN (UNII: 3SW678MX72) (Active Moiety)
- ONION (UNII: 492225Q21H)
- ONION (UNII: 492225Q21H) (Active Moiety)
- CALCIUM SULFIDE (UNII: 1MBW07J51Q)
- CALCIUM SULFIDE (UNII: 1MBW07J51Q) (Active Moiety)
- PHOSPHORUS (UNII: 27YLU75U4W)
- PHOSPHORUS (UNII: 27YLU75U4W) (Active Moiety)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- CHLORIDE ION (UNII: Q32ZN48698) (Active Moiety)
- ANEMONE PULSATILLA (UNII: I76KB35JEV)
- ANEMONE PULSATILLA (UNII: I76KB35JEV) (Active Moiety)
- MATRICARIA CHAMOMILLA (UNII: G0R4UBI2ZZ)
- MATRICARIA CHAMOMILLA (UNII: G0R4UBI2ZZ) (Active Moiety)
- GOLDENSEAL (UNII: ZW3Z11D0JV)
- GOLDENSEAL (UNII: ZW3Z11D0JV) (Active Moiety)
- SULFUR (UNII: 70FD1KFU70)
- SULFUR (UNII: 70FD1KFU70) (Active Moiety)
- SODIUM CATION (UNII: LYR4M0NH37) (Active Moiety)
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:
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)
- GLYCERIN (UNII: PDC6A3C0OX)
- WATER (UNII: 059QF0KO0R)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
* Please review the disclaimer below.
[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".