Mucus Relief

Product NDC: 71610-098
11-digit product format: 716100098
Labeler code: 71610
Product ID: 71610-098_34de35ef-20f0-4707-9f11-dcf8c4040796
Type: HUMAN OTC DRUG
Nonproprietary name: Guaifenesin 200 mg
Dosage form: TABLET
Route: ORAL
Labeler: Aphena Pharma Solutions - Tennessee, LLC
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

Reported adverse events (FAERS/openFDA)#

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

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
2ae3c1e1-2a12-444d-a763-590320d373e1	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
71610-098-18	Mucus Relief	3000 in 1 BOTTLE	TABLET	3000		2

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
71610-098-18	EA - Each	71610-098	ab528835-8bfa-4b5c-9ca8-22623f409e14	1	2018-12-13

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
71610-098	MUCUS RELIEF (GUAIFENESIN 200 MG) TABLET [APHENA PHARMA SOLUTIONS - TENNESSEE, LLC]	2	Current NDC, Legacy NDC, 1 package rows	20180831_2ae3c1e1-2a12-444d-a763-590320d373e1.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	Aphena Pharma Solutions - Tennessee, LLC	2ae3c1e1-2a12-444d-a763-590320d373e1	2018-07-18	Warnings	Exact identifier ndc (product): 71610-098

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	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
71610-098-18	71610009818	3000 TABLET in 1 BOTTLE (71610-098-18)	3000 tablet	2018-07-16	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Guaifenesin Caplets, 200 mg	Aphena Pharma Solutions - Tennessee, LLC	2018-07-18	HUMAN OTC DRUG LABEL	2