NDC11 54973328401

This exact 11-digit normalized identifier can correspond to more than one FDA hyphenation. FDA.report preserves the exact identifier and exposes every structurally valid candidate without guessing.

Possible FDA NDC forms#

Package NDC, Product root table
Package NDC	Product root
54973-3284-01	54973-3284
54973-3284-1	54973-3284

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 2 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
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	Hyland's Inc.	7979fc6f-6d2c-56c9-e053-2991aa0ac1f3	2023-08-23	Warnings	Exact identifier ndc (package): 54973-3284-1 ndc11 (package): 54973328401
BABY MUCUS PLUS COLD RELIEF	BRYONIA ALBA ROOT, EUPHRASIA STRICTA, CALCIUM SULFIDE, SODIUM CHLORIDE, PHOSPHORUS, ANEMONE PULSATILLA, RUMEX CRISPUS ROOT, AND SILICON DIOXIDE	Hyland's Inc.	d934cc8a-1e43-4942-858a-05b5d068679a	2023-08-22	Warnings	Exact identifier ndc (package): 54973-3284-1 ndc (product): 54973-3284 ndc11 (package): 54973328401

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.