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 49 of 178 · 3,550 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Diphenhydramine Hydrochloride	DIPHENHYDRAMINE HYDROCHLORIDE	Major Pharmaceuticals	04e70311-6412-4a20-84e3-f6e26d5f19ab	2026-02-20	Warnings	Exact identifier application number: M012
Banophen	DIPHENHYDRAMINE HCL	Major Pharmaceuticals	7f2b72cc-d4f7-431f-be61-c103cf8c489e	2026-02-20	Warnings	Exact identifier application number: M012
Diphenhydramine Hydrochloride	DIPHENHYDRAMINE HYDROCHLORIDE	Major Pharmaceuticals	dca04d80-e781-40b1-e053-2995a90a7010	2026-02-20	Warnings	Exact identifier application number: M012
Diphenhydramine Hydrochloride	DIPHENHYDRAMINE HYDROCHLORIDE	LEADER/ Cardinal Health 110, Inc.	e33cbd1d-1848-145a-e053-2995a90aeb50	2026-02-20	Warnings	Exact identifier application number: M012
Head Congestion and Flu Severe Relief	ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL	Rite Aid Corporation	416080a9-e817-485b-a4ae-6c9d0152c165	2026-02-20	Warnings	Exact identifier application number: M012
Walmart Dye Free Chidrens Allergy Chews	DIPHENHYDRAMINE HCL	WALMART STORES INC	18436026-b0e4-4481-a647-d735a27d0b00	2026-02-19	Warnings	Exact identifier application number: M012
Vaporizing	CAMPHOR	Meijer, Inc.	7afc98d7-f64f-42d5-9022-28ad6b01db8a	2026-02-19	Warnings, Adverse reactions	Exact identifier application number: M012
CHILDRENS COLD AND COUGH	BROMPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE	Kroger Company	8196b482-070e-4d7d-8943-129141f926ee	2026-02-19	Warnings	Exact identifier application number: M012
Walmart Dye Free Chidrens Allergy Chews Bubblegum	DIPHENHYDRAMINE HCL	WALMART STORES INC	9f83d2f0-9718-4f2b-bc7f-e29ba2917412	2026-02-19	Warnings	Exact identifier application number: M012
tussin dm max	DEXTROMETHORPHAN HBR, GUAIFENESIN	Kroger Company	be9aaf66-6c59-4042-88e2-acd920dcf992	2026-02-19	Warnings	Exact identifier application number: M012
Allergy Relief Dye-Free	DIPHENHYDRAMINE HCL	CVS Pharmacy	08459cf4-feb3-4283-88e1-d61e030c57f9	2026-02-19	Warnings	Exact identifier application number: M012
allergy relief	CHLORPHENIRAMINE MALEATE	Rite Aid Corporation	b0d70488-ea1d-4c1d-bd07-53dfb0e4d03c	2026-02-18	Warnings	Exact identifier application number: M012
Walgreens Wild Cherry Pectin Throat Drops	PECTIN	Walgreens	424fda2d-c1e5-0ed9-e063-6394a90a06ea	2026-02-18	Warnings	Exact identifier application number: M012
cough suppressant and topical analgesic	CAMPHOR, EUCALYPTUS OIL, MENTHOL	Target Corporation	df21d9d6-36a9-49cf-a29c-c4a573899bd5	2026-02-18	Warnings, Adverse reactions	Exact identifier application number: M012
Allergy Relief	CHLORPHENIRAMINE MALEATE	Amerisource Bergen	eeda80ff-212d-428e-a0c6-782f271357b4	2026-02-18	Warnings	Exact identifier application number: M012
good sense night time	ACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATE	L. Perrigo Company	e47dffdf-5778-4804-8ce2-54c5a72bba3a	2026-02-18	Warnings	Exact identifier application number: M012
Chest Rub	CAMPHOR, EUCALYPTUS OIL, MENTHOL	United Natural Foods, Inc. dba UNFI	b139e7d6-bf4d-45b9-b7cf-d34e5352095c	2026-02-17	Warnings, Adverse reactions	Exact identifier application number: M012
Chest Rub	CAMPHOR, EUCALYPTUS OIL, MENTHOL	Strategic Sourcing Services LLC	bd54bf7a-2304-4c3f-9cd2-bafea217466e	2026-02-17	Warnings, Adverse reactions	Exact identifier application number: M012
Creomulsion For Children	DEXTROMETHORPHAN HYDROBROMIDE	Socius Care, LLC	39d0e96c-1cc3-4961-e054-00144ff88e88	2026-02-17	Warnings	Exact identifier application number: M012
Creomulsion Cough Medicine Adult Formula	DEXTROMETHORPHAN HYDROBROMIDE	Socius Care, LLC	39d07486-99b7-5c06-e054-00144ff8d46c	2026-02-17	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