Baby Mucus Plus Cold Relief Daytime And Nighttime Kit
NDC 54973-3374

View dosage, usage, ingredients, routes, and UNII mappings.
Table of Contents
  1. Product Information
  2. Product Packages
  3. What is NDC 54973-3374?
  4. Baby Mucus Plus Cold Relief Daytime And Nighttime Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes

Product Information

Baby Mucus Plus Cold Relief Daytime And Nighttime (calcium sulfide,phosphorus,sulfur,rumex crispus root,sodium chloride,arabica coffee bean,anemone pulsatilla,silicon dioxide, goldenseal,onion,bryonia alba root,euphrasia stricta and matricaria chamomilla) is a UNAPPROVED HOMEOPATHIC-approved product labeled by Hyland's Inc.. This product is primarily utilized in pharmaceutical processing or compounding. It is supplied as a kit. This product entry covers the primary NDC 54973-3374 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.

Primary Identification

NDC Product Code:
54973-3374
Proprietary Name:
Baby Mucus Plus Cold Relief Daytime And Nighttime
Non-Proprietary Name: [1]
Calcium Sulfide, Phosphorus, Sulfur, Rumex Crispus Root, Sodium Chloride, Arabica Coffee Bean, Anemone Pulsatilla, Silicon Dioxide, Goldenseal, Onion, Bryonia Alba Root, Euphrasia Stricta And Matricaria Chamomilla
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Code Navigator:

Clinical Specifications

Dosage Form:
Kit - A packaged collection of related material.

Labeler & Regulatory Data

Labeler Name: [5]
Hyland's Inc.
Labeler Code:
54973
Product Label ID:
7979fc6f-6d2c-56c9-e053-2991aa0ac1f3
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.

Marketing Timeline

Start Marketing Date: [9]
11-01-2018
Listing Expiration Date: [11]
12-31-2026
Exclude Flag: [12]
N

Code Structure Chart

Product Details

What is NDC 54973-3374?

The NDC code 54973-3374 is assigned by the FDA to the product Baby Mucus Plus Cold Relief Daytime And Nighttime. It is commonly known by its generic name, calcium sulfide, phosphorus, sulfur, rumex crispus root, sodium chloride, arabica coffee bean, anemone pulsatilla, silicon dioxide, goldenseal, onion, bryonia alba root, euphrasia stricta and matricaria chamomilla. This pharmaceutical product is labeled by Hyland's Inc. and is currently categorized as listed product. The medication is a kit. In terms of distribution, this product is available in a single package configuration. The associated package NDC(s) include: 54973-3374-1. Beyond standard identification, this entry provides technical data including pharmacologic classes, UNII ingredient references, and RxNorm cross-referencing for healthcare systems.

What are the uses of this product?

• Measure only with the dosing syringe provided • Do not use dosing syringe with other products • On dosing syringe, mL = milliliter, tsp = teaspoon Measure only with the dosing syringe providedDo not use dosing syringe with other productsOn dosing syringe, mL = milliliter, tsp = teaspoonChildren under6 months of ageconsult a licensed health care professionalbefore using this productChildren 6 months tounder 1 year of age2.5 mL or ½ tsp at bedtime and every6 hours during the night or as necessaryChildren 1 to 3years of age5 mL or 1 tsp at bedtime and every 4 hoursduring the night or as necessary

Which are the associated UNII Codes?

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

Which are the Inactive Ingredients associated 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:

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Product & Regulatory Definitions
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.
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.
What is the Labeler Name? Name of Company corresponding to the labeler code segment of the Product NDC.
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.
What is the Start Marketing Date? This is the date that the labeler indicates was the start of its marketing of the drug product.
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.
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, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".