Mucus Relief

Product NDC: 17714-152
11-digit product format: 177140152
Labeler code: 17714
Product ID: 17714-152_5cc992c7-a1b3-46be-e053-2991aa0a1f8f
Type: HUMAN OTC DRUG
Nonproprietary name: Guaifenesin 400 mg
Dosage form: TABLET
Route: ORAL
Labeler: Advance Pharmaceutical Inc.
Application: part341
Marketing category: OTC MONOGRAPH FINAL
Marketing start: 2016-11-01
Substance: GUAIFENESIN
Active strength: 400 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	400 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
359601	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
5b78bbe9-806c-443f-bc23-351e5342355f	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
17714-152-01	Mucus Relief	100 in 1 BOTTLE	TABLET	100		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
17714-152	MUCUS RELIEF (GUAIFENESIN 400 MG) TABLET [ADVANCE PHARMACEUTICAL INC.]	2	Current NDC, Legacy NDC, 1 package rows	20171031_5b78bbe9-806c-443f-bc23-351e5342355f.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 400 MG	Advance Pharmaceutical Inc.	5b78bbe9-806c-443f-bc23-351e5342355f	2017-10-30	Warnings	Exact identifier ndc (product): 17714-152

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
359601	guaiFENesin 400 MG Oral Tablet	PSN	5b78bbe9-806c-443f-bc23-351e5342355f	2
359601	guaifenesin 400 MG Oral Tablet	SCD	5b78bbe9-806c-443f-bc23-351e5342355f	2

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
17714-152-01	17714015201	100 TABLET in 1 BOTTLE (17714-152-01)	100 tablet	2016-11-01	0000-00-00	No	No	Current