NDC 53499-2137 Umcka Coldcare Starter Kit
Kit - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 53499 - Schwabe North America, Inc.
- 53499-2137 - Umcka Coldcare Starter Kit
Product Characteristics
LEMON (C73396)
Product Packages
NDC Code 53499-2137-1
Package Description: 1 KIT in 1 CARTON * 1 BOTTLE, PLASTIC in 1 CARTON (53499-5273-5) / 120 mL in 1 BOTTLE, PLASTIC * 10 PACKET in 1 CARTON (53499-5146-0) / 5 g in 1 PACKET
Product Details
What is NDC 53499-2137?
What are the uses for Umcka Coldcare Starter Kit?
Which are Umcka Coldcare Starter Kit UNII Codes?
The UNII codes for the active ingredients in this product are:
- PELARGONIUM SIDOIDES ROOT (UNII: H6J53HEX8E)
- PELARGONIUM SIDOIDES ROOT (UNII: H6J53HEX8E) (Active Moiety)
Which are Umcka Coldcare Starter Kit 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:
- ARONIA MELANOCARPA FRUIT JUICE (UNII: D2EVP827PJ)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- ALCOHOL (UNII: 3K9958V90M)
- FRUCTOSE (UNII: 6YSS42VSEV)
- MALTODEXTRIN (UNII: 7CVR7L4A2D)
- POTASSIUM CITRATE (UNII: EE90ONI6FF)
- WATER (UNII: 059QF0KO0R)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- TURMERIC (UNII: 856YO1Z64F)
- XYLITOL (UNII: VCQ006KQ1E)
* 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".