54973-3374 NDC - 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)

Drug Information

Product NDC: 54973-3374
Proprietary Name: BABY MUCUS PLUS COLD RELIEF DAYTIME AND NIGHTTIME
Non Proprietary 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
Active Ingredient(s):
Administration Route(s):
Dosage Form(s): KIT

Labeler Information

Field Name	Field Value
Labeler Name:	Hyland's Inc.
Product Type:	HUMAN OTC DRUG
FDA Application Number:
Marketing Category:	UNAPPROVED HOMEOPATHIC
Start Marketing Date:	11/1/2018

Package Information

No.	Package Code	Package Description	Billing Unit
1	54973-3374-1	1 KIT in 1 CARTON (54973-3374-1) * 118 mL in 1 BOTTLE, PLASTIC (54973-3284-1) * 118 mL in 1 BOTTLE (54973-3371-2)

NDC Record

Field Name	Field Value	Definition
PRODUCT NDC	54973-3374	The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAME	HUMAN OTC DRUG	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.
PROPRIETARY NAME	BABY MUCUS PLUS COLD RELIEF DAYTIME AND NIGHTTIME	The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY 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	The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAME	KIT	The translation of the dosage form Code submitted by the firm.
START MARKETING DATE	11/1/2018	This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAME	UNAPPROVED HOMEOPATHIC	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.
LABELER NAME	Hyland's Inc.	Name of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 2/5/2026

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