Baby Mucus Plus Cold Relief Liquid
NDC Package 54973-3284-2

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

Package Information

Baby Mucus Plus Cold Relief (bryonia alba root, euphrasia stricta, calcium sulfide, sodium chloride, phosphorus, anemone pulsatilla, rumex crispus root, and silicon dioxide) liquids is • 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. This formulation utilizes a liquid delivery system. Marketed by Hyland's Inc., this product is identified by NDC 54973-3284.

Identification & Billing

NDC Package Code
54973-3284-2
Package Description
2.5 mL in 1 POUCH
Product Code
54973-3284
11-Digit Billing Format
54973328402

Clinical Specifications

Proprietary Name
Baby Mucus Plus Cold Relief
Non-Proprietary Name
Bryonia Alba Root, Euphrasia Stricta, Calcium Sulfide, Sodium Chloride, Phosphorus, Anemone Pulsatilla, Rumex Crispus Root, And Silicon Dioxide
Substance Name
Anemone Pulsatilla; Bryonia Alba Root; Calcium Sulfide; Euphrasia Stricta; Phosphorus; Rumex Crispus Root; Silicon Dioxide; Sodium Chloride
Dosage Form
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Administration Route
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
Pharmacologic Class
Usage Information
• 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

Regulatory & Marketing

Labeler Name
Hyland's Inc.
Product Type
Human Otc Drug
Marketing Category
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date
05-13-2016
Listing Expiration
12-31-2026
Exclude Flag
N
Sample Package
Yes

Hierarchy Structure

Code Lineage

The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

* Please review the full disclaimer at the bottom of this page.

Other Available Packages

The following commercial packages are registered under the same Product NDC (54973-3284). Click a package code to view its specific billing and regulatory data.

54973-3284-1
1 BOTTLE, PLASTIC in 1 CARTON / 118 mL in 1 BOTTLE, PLASTIC
54973-3284-3
1 BOTTLE, PLASTIC in 1 CARTON / 148 mL in 1 BOTTLE, PLASTIC

* Please review the full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 54973-3284-2 identifies a specific commercial package of 2.5 ml in 1 pouch of Baby Mucus Plus Cold Relief, a human over the counter drug labeled by Hyland's Inc.. This liquid is formulated for oral use and contains anemone pulsatilla; bryonia alba root; calcium sulfide; euphrasia stricta; phosphorus; rumex crispus root; silicon dioxide; sodium chloride as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Hyland's Inc. on May 13, 2016. The current certification is valid through December 31, 2026.

How is this Hyland's Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 54973328402. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-4-1)
54973-3284-2
11-Digit CMS (5-4-2)
54973-3284-02

Note: The zero is added to the Package segment to maintain the 5-4-2 structure.