1. Home
  2. Labeler Index
  3. Hyland's Inc.
  4. NDC Product Code: 54973-4059 Kids Cough And Mucus Day And Night Grape

NDC 54973-4059 Kids Cough And Mucus Day And Night Grape

Rumex Crispus Root,Antimony Potassium Tartrate,Bryonia Alba Root,Matricaria Chamomilla - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 54973-4059?
  5. Kids Cough And Mucus Day And Night Grape Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes

Product Information

NDC Product Code:
54973-4059
Proprietary Name:
Kids Cough And Mucus Day And Night Grape
Non-Proprietary Name: [1]
Rumex Crispus Root, Antimony Potassium Tartrate, Bryonia Alba Root, Matricaria Chamomilla Whole, Pulsatilla Vulgaris, Calcium Sulfide, Ipecac, Goldenseal, Phosphorus, Ferrosoferric Phosphate
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]
Hyland's Inc.
Labeler Code:
54973
Product Label ID:
d92ab90b-b960-3df2-e053-2a95a90ace89
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date: [9]
03-01-2022
Listing Expiration Date: [11]
12-31-2024
Exclude Flag: [12]
N
Code Structure:
Code Navigator:

Product Characteristics

Flavor(s):
GRAPE (C73391)

Product Packages

NDC Code 54973-4059-1

Package Description: 1 KIT in 1 CARTON * 1 BOTTLE, PLASTIC in 1 CARTON (54973-4057-1) / 118 mL in 1 BOTTLE, PLASTIC * 1 BOTTLE, PLASTIC in 1 CARTON (54973-4056-1) / 118 mL in 1 BOTTLE, PLASTIC

Product Details

What is NDC 54973-4059?

The NDC code 54973-4059 is assigned by the FDA to the product Kids Cough And Mucus Day And Night Grape which is a human over the counter drug product labeled by Hyland's Inc.. The generic name of Kids Cough And Mucus Day And Night Grape is rumex crispus root, antimony potassium tartrate, bryonia alba root, matricaria chamomilla whole, pulsatilla vulgaris, calcium sulfide, ipecac, goldenseal, phosphorus, ferrosoferric phosphate. The product's dosage form is kit. The product is distributed in a single package with assigned NDC code 54973-4059-1 1 kit in 1 carton * 1 bottle, plastic in 1 carton (54973-4057-1) / 118 ml in 1 bottle, plastic * 1 bottle, plastic in 1 carton (54973-4056-1) / 118 ml in 1 bottle, plastic. 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 Kids Cough And Mucus Day And Night Grape?

■ Use as directed. ■ Do not refrigerate. ■ Shake well before using. ■ Measure only with the dosing cup provided. ■ Do not use dosing cup with other products. ■ On dosing cup, mL = milliliter. Children 2 years to under 6 years 5 mL up to 6 times per day (every 4 hours). Children 6 years to under 12 years 10 mL up to 6 times per day (every 4 hours). Adults and children 12 years and over 15 mL up to 6 times per day (every 4 hours). ■ Use as directed. ■ Do not refrigerate. ■ Shake well before using. ■ Measure only with the dosing cup provided. ■ Do not use dosing cup with other products. ■ On dosing cup, mL = milliliter. Children 2 years to under 6 years 5 mL at bedtime and every 4 hours during the night until relieved. Children 6 years to under 12 years 10 mL at bedtime and every 4 hours during the night until relieved. Adults and children 12 years and over 15 mL at bedtime and every 4 hours during the night until relieved.

Which are Kids Cough And Mucus Day And Night Grape UNII Codes?

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

Which are Kids Cough And Mucus Day And Night Grape 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".