MUCUS RELIEF

Product NDC: 57896-714
11-digit product format: 578960714
Labeler code: 57896
Product ID: 57896-714_43d0077d-5ba5-88af-e063-6294a90a62aa
Type: HUMAN OTC DRUG
Nonproprietary name: Guaifenesin
Dosage form: TABLET
Route: ORAL
Labeler: Geri-Care Pharmaceuticals, Corp
Application: M012
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2021-02-01
Substance: GUAIFENESIN
Active strength: 400 mg/1
Pharmacologic classes: Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE]
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	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
c5ea5a7a-c806-e5e0-e053-2995a90a15e9	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
57896-714-01	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
57896-714-01	EA - Each	57896-714	cf7a3043-4418-41b2-9ea9-2167db2b9ec1	1	2021-10-08

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
57896-714	MUCUS RELIEF (GUAIFENESIN) TABLET [GERI-CARE PHARMACEUTICALS, CORP]	2	Current NDC, Legacy NDC, 1 package rows	20231026_c5ea5a7a-c806-e5e0-e053-2995a90a15e9.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 110 of 180 · 3,583 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Defensol D Blister Pack	ACETAMINOPHEN, DIPHENHYDRAMINE HCL, PHENYLEPHRINE HCI	Menper Distributors, Inc.	0dfcc977-6101-4536-e063-6294a90a7a48	2025-07-22	Warnings	Exact identifier application number: M012
Broncofin	DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCL	Menper Distributors, Inc.	fdf67382-1692-485b-92f1-2cbb8be4fb70	2025-07-22	Warnings	Exact identifier application number: M012
Defensol Adult Syrup	GUAIFENESIN, DEXTROMETHORPHAN HBR	Menper Distributors, Inc.	62acff69-8c40-4a0e-8d56-be2cc14e3d45	2025-07-22	Warnings	Exact identifier application number: M012
Cosedal Drops	DEXTROMETHORPHAN HBR, GUAIFENESIN	Menper Distributors, Inc.	1241d249-ea3b-4d2b-87ed-835d6a2d286a	2025-07-22	Warnings	Exact identifier application number: M012
Berro y Cebolla DM	DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN	Menper Distributors, Inc.	20107bd9-6d84-4ab5-a0d9-966f1f11d919	2025-07-22	Warnings	Exact identifier application number: M012
Defensol-ito	DEXTROMETHORPHAN, GUIAFENESIN, PHENYLEPHRINE	Menper Distributors, Inc	a7c7a60d-d49f-4239-92f7-714eac7eb0c5	2025-07-22	Warnings	Exact identifier application number: M012
Bisolvine Children	GUAIFENESIN, DEXTROMETHORPHAN	MENPER DISTRIBUTORS INC.	896a5443-e3d2-4af7-9e27-f1c1899ce038	2025-07-22	Warnings	Exact identifier application number: M012
Bisolvine Aloe-Miel	DEXTROMETHORPHAN, GUAIFENESIN	MENPER DISTRIBUTORS INC.	34801c79-ce88-492f-808e-b639e8601607	2025-07-22	Warnings	Exact identifier application number: M012
Viva Porru Chest Rub	CAMPHOR, MENTHOL, EUCALYPTUS OIL	Menper Distributors, Inc.	0dfadfe3-9e40-0eee-e063-6294a90a00c3	2025-07-22	Warnings	Exact identifier application number: M012
leader childrens allergy relief	DIPHENHYDRAMINE HCL	Cardinal Health 110, LLC. dba Leader	40d697b7-dc59-4d24-8d46-db635e01b9d5	2025-07-22	Warnings	Exact identifier application number: M012
Allergy Relief	CHLORPHENIRAMINE MALEATE	Chain Drug Consortium	34005c55-3176-4f28-9a3b-7dc6fefd01fe	2025-07-19	Warnings	Exact identifier application number: M012
Sinus Relief Daytime Nighttime	ACETAMINOPHEN, DIPHENHYDRAMINE HCL, GUAIFENESIN, PHENYLEPHRINE HCL	Kroger Company	73a77a13-983b-4e65-bb3c-2ba5e9f33a3e	2025-07-19	Warnings	Exact identifier application number: M012
QUALITY CHOICE No Drip Nasal Mist	OXYMETAZOLINE HYDROCHLORIDE	QUALITY CHOICE (CHAIN DRUG MARKETING ASSOCIATION)	7cb6ad04-7847-46b9-b371-0a3473001c79	2025-07-18	Warnings	Exact identifier application number: M012
Nasal Decongestant Maximum Strength	PSEUDOEPHEDRINE HCL	Chain Drug Consortium	270e9221-d305-4148-b523-741e02fe733f	2025-07-18	Warnings	Exact identifier application number: M012
ACTISPEC PSE	DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PSEUDOEPHEDRINE HYDROCHLORIDE	ACTIPHARMA, LLC	5def1555-87f4-41d5-8a5c-be560aa8f1e2	2025-07-17	Warnings	Exact identifier application number: M012
EXTRA STRENGTH TYLENOL SEVERE COUGH PLUS SORE THROAT DAY	ACETAMINOPHEN AND DEXTROMETHORPHAN HYDROBROMIDE	Kenvue Brands LLC	1a17b24a-8022-4e2f-e063-6294a90af276	2025-07-17	Warnings	Exact identifier application number: M012
BULPOL Smoking Patches	MENTHOL	Jiashen International Trade Limited	3a1cc0e1-fabf-52b9-e063-6394a90ae35e	2025-07-17	Warnings	Exact identifier application number: M012
Ampigrin Ultra Forte Night	ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE	OPMX LLC	e11e71c3-fe7c-77c7-e053-2995a90a34b2	2025-07-17	Warnings	Exact identifier application number: M012
Nitecin	ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE	OPMX LLC	dfb56532-6f72-1e4d-e053-2a95a90a1c05	2025-07-17	Warnings	Exact identifier application number: M012
tabcin NIGHT	ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE	OPMX LLC	0b3ed2bb-88ed-699e-e063-6394a90ac023	2025-07-17	Warnings	Exact identifier application number: M012

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	c5ea5a7a-c806-e5e0-e053-2995a90a15e9	3
359601	guaifenesin 400 MG Oral Tablet	SCD	c5ea5a7a-c806-e5e0-e053-2995a90a15e9	3
359601	guaiFENesin 400 MG Oral Tablet	PSN	761825bc-f835-4947-bfa0-2940f1dff5fb	1
359601	guaifenesin 400 MG Oral Tablet	SCD	761825bc-f835-4947-bfa0-2940f1dff5fb	1

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
57896-714-01	57896071401	100 TABLET in 1 BOTTLE (57896-714-01)	100 tablet	2021-02-01	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
gc 714	Bryant Ranch Prepack	2026-04-17	HUMAN OTC DRUG LABEL	1
gc 714	Geri-Care Pharmaceuticals, Corp	2025-11-17	HUMAN OTC DRUG LABEL	3