MUCOSA

Product NDC: 49483-272
11-digit product format: 494830272
Labeler code: 49483
Product ID: 49483-272_092526a7-c2e1-4cb5-e063-6394a90ac509
Type: HUMAN OTC DRUG
Nonproprietary name: GUAIFENESIN
Dosage form: TABLET
Route: ORAL
Labeler: TIME CAP LABORATORIES,INC
Application: M012
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2012-04-16
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: MUCOSA
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
d34ef2e8-adc2-48e5-a572-e354937daec6	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	SPL version
49483-272-00	MUCOSA	100000 in 1 CARTON	TABLET	100000	5
49483-272-06	MUCOSA	60 in 1 BOTTLE, PLASTIC	TABLET	60	5
49483-272-20	MUCOSA	200 in 1 BOTTLE	TABLET	200	5

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
49483-272-06	EA - Each	49483-272	58558786-c85e-40fc-96a2-3b3579028fcd	1	2012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
GUAIFENESIN	ACTIVE INGREDIENT	495W7451VQ	MUCOSA (GUAIFENESIN) TABLET [AVPAK]	2
GUAIFENESIN	ACTIVE INGREDIENT	495W7451VQ	MUCOSA (GUAIFENESIN) TABLET [TIME CAP LABORATORIES,INC]	2
GUAIFENESIN	ACTIVE MOIETY	495W7451VQ	MUCOSA (GUAIFENESIN) TABLET [AVPAK]	2
GUAIFENESIN	ACTIVE MOIETY	495W7451VQ	MUCOSA (GUAIFENESIN) TABLET [TIME CAP LABORATORIES,INC]	2
CELLULOSE, MICROCRYSTALLINE	INACTIVE INGREDIENT	OP1R32D61U	MUCOSA (GUAIFENESIN) TABLET [TIME CAP LABORATORIES,INC]	2
CELLULOSE, MICROCRYSTALLINE	INACTIVE INGREDIENT	OP1R32D61U	MUCOSA (GUAIFENESIN) TABLET [AVPAK]	2
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	MUCOSA (GUAIFENESIN) TABLET [TIME CAP LABORATORIES,INC]	2
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	MUCOSA (GUAIFENESIN) TABLET [AVPAK]	2
MALTODEXTRIN	INACTIVE INGREDIENT	7CVR7L4A2D	MUCOSA (GUAIFENESIN) TABLET [TIME CAP LABORATORIES,INC]	2
MALTODEXTRIN	INACTIVE INGREDIENT	7CVR7L4A2D	MUCOSA (GUAIFENESIN) TABLET [AVPAK]	2
POVIDONE	INACTIVE INGREDIENT	FZ989GH94E	MUCOSA (GUAIFENESIN) TABLET [TIME CAP LABORATORIES,INC]	2
Povidones	INACTIVE INGREDIENT	FZ989GH94E	MUCOSA (GUAIFENESIN) TABLET [AVPAK]	2
SILICON DIOXIDE	INACTIVE INGREDIENT	ETJ7Z6XBU4	MUCOSA (GUAIFENESIN) TABLET [TIME CAP LABORATORIES,INC]	2
SILICON DIOXIDE	INACTIVE INGREDIENT	ETJ7Z6XBU4	MUCOSA (GUAIFENESIN) TABLET [AVPAK]	2
Sodium Starch Glycolate Type A Potato	INACTIVE INGREDIENT	5856J3G2A2	MUCOSA (GUAIFENESIN) TABLET [AVPAK]	2
SODIUM STARCH GLYCOLATE TYPE A POTATO	INACTIVE INGREDIENT	5856J3G2A2	MUCOSA (GUAIFENESIN) TABLET [TIME CAP LABORATORIES,INC]	2
STEARIC ACID	INACTIVE INGREDIENT	4ELV7Z65AP	MUCOSA (GUAIFENESIN) TABLET [TIME CAP LABORATORIES,INC]	2
STEARIC ACID	INACTIVE INGREDIENT	4ELV7Z65AP	MUCOSA (GUAIFENESIN) TABLET [AVPAK]	2
GUAIFENESIN	ACTIVE INGREDIENT	495W7451VQ	MUCUS RELIEF (GUAIFENESIN) TABLET [MAJOR PHARMACEUTICALS INC]	1
GUAIFENESIN	ACTIVE INGREDIENT	495W7451VQ	MUCUS RELIEF (GUAIFENESIN) TABLET [CLINICAL SOLUTIONS WHOLESALE]	1
GUAIFENESIN	ACTIVE MOIETY	495W7451VQ	MUCUS RELIEF (GUAIFENESIN) TABLET [MAJOR PHARMACEUTICALS INC]	1
GUAIFENESIN	ACTIVE MOIETY	495W7451VQ	MUCUS RELIEF (GUAIFENESIN) TABLET [CLINICAL SOLUTIONS WHOLESALE]	1
CELLULOSE, MICROCRYSTALLINE	INACTIVE INGREDIENT	OP1R32D61U	MUCUS RELIEF (GUAIFENESIN) TABLET [CLINICAL SOLUTIONS WHOLESALE]	1
CELLULOSE, MICROCRYSTALLINE	INACTIVE INGREDIENT	OP1R32D61U	MUCUS RELIEF (GUAIFENESIN) TABLET [MAJOR PHARMACEUTICALS INC]	1
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	MUCUS RELIEF (GUAIFENESIN) TABLET [MAJOR PHARMACEUTICALS INC]	1
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	MUCUS RELIEF (GUAIFENESIN) TABLET [CLINICAL SOLUTIONS WHOLESALE]	1
MALTODEXTRIN	INACTIVE INGREDIENT	7CVR7L4A2D	MUCUS RELIEF (GUAIFENESIN) TABLET [MAJOR PHARMACEUTICALS INC]	1
MALTODEXTRIN	INACTIVE INGREDIENT	7CVR7L4A2D	MUCUS RELIEF (GUAIFENESIN) TABLET [CLINICAL SOLUTIONS WHOLESALE]	1
POVIDONE	INACTIVE INGREDIENT	FZ989GH94E	MUCUS RELIEF (GUAIFENESIN) TABLET [MAJOR PHARMACEUTICALS INC]	1
POVIDONES	INACTIVE INGREDIENT	FZ989GH94E	MUCUS RELIEF (GUAIFENESIN) TABLET [CLINICAL SOLUTIONS WHOLESALE]	1
SILICON DIOXIDE	INACTIVE INGREDIENT	ETJ7Z6XBU4	MUCUS RELIEF (GUAIFENESIN) TABLET [MAJOR PHARMACEUTICALS INC]	1
SILICON DIOXIDE	INACTIVE INGREDIENT	ETJ7Z6XBU4	MUCUS RELIEF (GUAIFENESIN) TABLET [CLINICAL SOLUTIONS WHOLESALE]	1
SODIUM STARCH GLYCOLATE TYPE A POTATO	INACTIVE INGREDIENT	5856J3G2A2	MUCUS RELIEF (GUAIFENESIN) TABLET [MAJOR PHARMACEUTICALS INC]	1
SODIUM STARCH GLYCOLATE TYPE A POTATO	INACTIVE INGREDIENT	5856J3G2A2	MUCUS RELIEF (GUAIFENESIN) TABLET [CLINICAL SOLUTIONS WHOLESALE]	1
STEARIC ACID	INACTIVE INGREDIENT	4ELV7Z65AP	MUCUS RELIEF (GUAIFENESIN) TABLET [MAJOR PHARMACEUTICALS INC]	1
STEARIC ACID	INACTIVE INGREDIENT	4ELV7Z65AP	MUCUS RELIEF (GUAIFENESIN) TABLET [CLINICAL SOLUTIONS WHOLESALE]	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
49483-272	MUCOSA (GUAIFENESIN) TABLET [TIME CAP LABORATORIES,INC]	5	Current NDC, Legacy NDC, 3 package rows	20231102_d34ef2e8-adc2-48e5-a572-e354937daec6.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 37 of 178 · 3,551 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Severe Cold and Flu Night time	ACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATE, PHENYLEPHRINE HCL	HyVee Inc	4f963491-e1f0-494d-acb6-5f4d2b267d4a	2026-04-22	Warnings	Exact identifier application number: M012
Vicks Sinex SEVERE MOISTURIZING ULTRA FINE MIST	OXYMETAZOLINE HYDROCHLORIDE	Procter & Gamble Manufacturing GmbH	f4b01827-7444-3bfc-e053-2a95a90aebed	2026-04-22	Warnings	Exact identifier application number: M012
Vicks Sinex SEVERE ORIGINAL ULTRA FINE MIST	OXYMETAZOLINE HYDROCHLORIDE	Procter & Gamble Manufacturing GmbH,	cfd43b8f-8064-6b88-e053-2a95a90a329e	2026-04-22	Warnings	Exact identifier application number: M012
Vicks Sinex Severe Original	OXYMETAZOLINE HYDROCHLORIDE	Procter & Gamble Manufacturing GmbH	cfd048c9-2f33-101d-e053-2995a90ad854	2026-04-22	Warnings	Exact identifier application number: M012
Vicks Sinex SEVERE VapoCOOL ULTRA FINE MIST	OXYMETAZOLINE HYDROCHLORIDE	Procter & Gamble Manufacturing GmbH	d0768332-7c24-7c30-e053-2a95a90a26d4	2026-04-22	Warnings	Exact identifier application number: M012
Histanaz	PSEUDOEPHEDRINE HCL, PYRILAMINE MALEATE	Capital Pharmaceutical, LLC	3e87d0f3-f16c-5972-e063-6294a90acc8a	2026-04-22	Warnings	Exact identifier application number: M012
Good Sense Severe Daytime Cold and Flu	ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL	L. Perrigo Company	d5faf89f-3641-4be1-8d43-35504f12fe8d	2026-04-22	Warnings	Exact identifier application number: M012
Multi-Symptom Cold childrens	DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL	WALMART INC.	5ee5eb75-fc56-42a1-bf2c-b9c10ea8bfd4	2026-04-22	Warnings	Exact identifier application number: M012
good sense nasal	OXYMETAZOLINE HYDROCHLORIDE	L. Perrigo Company	95f23049-e523-4c59-904c-b8e9ae82602c	2026-04-22	Warnings	Exact identifier application number: M012
Mucinex Childrens FreeFrom Multi-Symptom Cold and Stuffy Nose	DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, AND PHENYLEPHRINE HYDROCHLORIDE	Reckitt Benckiser LLC	c07dad99-87b0-419b-9230-7c22a77ecf9e	2026-04-21	Warnings	Exact identifier application number: M012
Cough and Cold HBP	CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HBR	Valu Merchandisers Company	83db90da-9155-4f6a-8209-44c87d14b696	2026-04-21	Warnings	Exact identifier application number: M012
Pain, Headache and Cough	ACETAMINOPHEN, DEXTROMETHORPHAN HBR	CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED	613a2516-fc61-4bb4-bd44-ca6004548193	2026-04-21	Warnings	Exact identifier application number: M012
Dr. Simi Allergy Relief	DIPHENHYDRAMINE HCL	Farmacias De Similares TX LLC	4fe8bbe3-13c9-5458-e063-6294a90a9064	2026-04-20	Warnings	Exact identifier application number: M012
Cold and Flu Day and Night, Severe	ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL	ARMY AND AIR FORCE EXCHANGE SERVICE	58d722ef-db67-44ac-a295-dd10e1f5ca1d	2026-04-20	Warnings	Exact identifier application number: M012
Loratadine 10mg	LORATADINE	BETTER LIVING BRANDS, LLC	46d615dd-45d5-2dfc-e063-6394a90a5d42	2026-04-18	Warnings	Exact identifier application number: M012
Multi-Symptom Cold Daytime	ACETAMINOPHEN, DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCL	Valu Merchandisers Company	d0f896a6-5637-45ef-bf60-b343cbcdcf7e	2026-04-17	Warnings	Exact identifier application number: M012
MUCUS RELIEF	GUAIFENESIN	Bryant Ranch Prepack	9ed5611f-4e1d-4f71-b430-a2a949bf7fe5	2026-04-17	Warnings	Exact identifier application number: M012
Multi-Symptom Cold	ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCL	Valu Merchandisers Company	bf3158af-89ab-4b7c-9f39-0f316fbe9056	2026-04-17	Warnings	Exact identifier application number: M012
MUCUS RELIEF	GUAIFENESIN	Bryant Ranch Prepack	761825bc-f835-4947-bfa0-2940f1dff5fb	2026-04-17	Warnings	Exact identifier application number: M012
equate cold and flu	ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE	WALMART INC.	e83d14cc-9b90-40ce-a00a-2702d8a8968f	2026-04-17	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	d34ef2e8-adc2-48e5-a572-e354937daec6	5
359601	guaifenesin 400 MG Oral Tablet	SCD	d34ef2e8-adc2-48e5-a572-e354937daec6	5
359601	guaiFENesin 400 MG Oral Tablet	PSN	33f9c655-87f5-4cbb-889f-fbb3f376b09d	4
359601	guaifenesin 400 MG Oral Tablet	SCD	33f9c655-87f5-4cbb-889f-fbb3f376b09d	4
359601	guaiFENesin 400 MG Oral Tablet	PSN	73f68f97-ad3a-492b-a96d-304b464ffd03	1
359601	guaifenesin 400 MG Oral Tablet	SCD	73f68f97-ad3a-492b-a96d-304b464ffd03	1

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
49483-272-00	49483027200	100000 TABLET in 1 CARTON (49483-272-00)	100000 tablet	2012-04-16	0000-00-00	No	No	Current
49483-272-06	49483027206	60 TABLET in 1 BOTTLE, PLASTIC (49483-272-06)	60 tablet	2012-04-16	0000-00-00	No	No	Current
49483-272-20	49483027220	200 TABLET in 1 BOTTLE (49483-272-20)	200 tablet	2023-09-15		No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
272R Timely 49483-272 Guaifenesin 400 mg Tablets	TIME CAP LABORATORIES,INC	2023-11-02	HUMAN OTC DRUG LABEL	5
major 272R	Major Pharmaceuticals \| TIME CAP LABORATORIES, INC	2019-12-04	HUMAN OTC DRUG LABEL	5
Guaifenesin (Product contract packaged by Apace Packaging, LLC)	Apace Packaging, LLC \| Time Cap Laboratories, Inc.	2018-11-20	HUMAN OTC DRUG LABEL	2
Guaifenesin	AvPAK	2018-06-07	HUMAN OTC DRUG LABEL	3
MUCOSA - Unit Dose Services	Unit Dose Services	2017-07-19	HUMAN OTC DRUG LABEL	4
Mucus Relief 400mg	Clinical Solutions Wholesale	2013-11-20	HUMAN OTC DRUG LABEL	1