NDC 83102-1060 Umcka Coldcare Day Plus Night
Umcka Coldcare Day Plus Night Kit

Product Information

What is NDC 83102-1060?

The NDC code 83102-1060 is assigned by the FDA to the product Umcka Coldcare Day Plus Night which is a human over the counter drug product labeled by Prosolutions Inc.. The generic name of Umcka Coldcare Day Plus Night is umcka coldcare day plus night. The product's dosage form is kit and is administered via form. The product is distributed in a single package with assigned NDC code 83102-1060-1 1 kit in 1 carton * 8 pouch in 1 package (83102-1040-1) / 5 g in 1 pouch * 4 pouch in 1 package (83102-1050-1) / 5 g in 1 pouch. This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information, RxNorm crosswalk and the complete product label.

NDC Product Code83102-1060
Proprietary Name What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.		Umcka Coldcare Day Plus Night
Non-Proprietary Name 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.		Umcka Coldcare Day Plus Night
Product Type 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.		Human Otc Drug
Dosage FormKit - A packaged collection of related material.
Product Labeler Information What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.		Prosolutions Inc.
Labeler Code83102
Marketing Category 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.		UNAPPROVED HOMEOPATHIC -
Start Marketing Date What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.		03-01-2023
Listing Expiration Date 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.		12-31-2024
Exclude Flag 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". 		N
NDC Code Structure

Product Characteristics

Flavor(s)LEMON (C73396)
CITRUS (C73378)
HONEY (C73394)

Product Packages

NDC Code 83102-1060-1

Package Description: 1 KIT in 1 CARTON * 8 POUCH in 1 PACKAGE (83102-1040-1) / 5 g in 1 POUCH * 4 POUCH in 1 PACKAGE (83102-1050-1) / 5 g in 1 POUCH

Product Details

Umcka Coldcare Day Plus Night Active Ingredients UNII Codes

Umcka Coldcare Day Plus Night 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.

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Umcka Coldcare Day Plus Night Product Label

FDA filings in the form of structured product labels are documents that include all published material associated whith this product. Product label information includes data like indications and usage generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Label Table of Contents



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