Mucus Relief

Product NDC: 54738-980
11-digit product format: 547380980
Labeler code: 54738
Product ID: 54738-980_73570295-8ab7-1c19-e053-2991aa0a6b82
Type: HUMAN OTC DRUG
Nonproprietary name: Guaifenesin 200 mg
Dosage form: TABLET
Route: ORAL
Labeler: Richmond Pharmaceuticals, Inc.
Application: part341
Marketing category: OTC MONOGRAPH FINAL
Marketing start: 2016-03-01
Substance: GUAIFENESIN
Active strength: 200 mg/1
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

Additional Listing Data#

Finished product: Yes
Brand name base: Mucus Relief
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
GUAIFENESIN	200 mg/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
495W7451VQ	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
197741	Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
e20927a1-d402-48c1-ba00-0745ddd0a0e7	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
4fe95224-f543-4dbb-9445-8cca122b48c8	Product name	1	20150609
e8718272-64cb-4436-969b-176c3067c8f4	Product name	1	20150609
106ff02a-57e1-4c4c-a307-fd582ff4e311	Product name	1	20150212

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
54738-980-01	Mucus Relief	100 in 1 BOTTLE	TABLET	100		3

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
54738-980-01	EA - Each	54738-980	f24d3295-afaf-4963-a895-28054d78ef6b	1	2017-11-06

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
54738-980	MUCUS RELIEF (GUAIFENESIN 200 MG) TABLET [RICHMOND PHARMACEUTICALS, INC.]	3	Current NDC, Legacy NDC, 1 package rows	20180822_e20927a1-d402-48c1-ba00-0745ddd0a0e7.zip

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 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Mucus Relief	GUAIFENESIN 200 MG	Richmond Pharmaceuticals, Inc.	e20927a1-d402-48c1-ba00-0745ddd0a0e7	2018-08-13	Warnings	Exact identifier ndc (product): 54738-980

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
495W7451VQ	GUAIFENESIN	93-14-1	GUAIFENESIN

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
197741	guaiFENesin 200 MG Oral Tablet	PSN	e20927a1-d402-48c1-ba00-0745ddd0a0e7	3
197741	guaifenesin 200 MG Oral Tablet	SCD	e20927a1-d402-48c1-ba00-0745ddd0a0e7	3
197741	guaiFENesin 200 MG Oral Tablet	PSN	2ae3c1e1-2a12-444d-a763-590320d373e1	2
197741	guaifenesin 200 MG Oral Tablet	SCD	2ae3c1e1-2a12-444d-a763-590320d373e1	2

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
54738-980-01	54738098001	100 TABLET in 1 BOTTLE (54738-980-01)	100 tablet	2016-03-01	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Guaifenesin Caplets, 200 mg	Richmond Pharmaceuticals, Inc. \| Advance Pharmaceutical Inc.	2018-08-13	HUMAN OTC DRUG LABEL	3
Guaifenesin Caplets, 200 mg	Aphena Pharma Solutions - Tennessee, LLC	2018-07-18	HUMAN OTC DRUG LABEL	2