Chest Congestion Relief

Product NDC: 49348-729
11-digit product format: 493480729
Labeler code: 49348
Product ID: 49348-729_6c8c7db1-ed1b-4499-ab97-296c6e8fac32
Type: HUMAN OTC DRUG
Nonproprietary name: Guaifenesin
Dosage form: TABLET
Route: ORAL
Labeler: Strategic Sourcing Services LLC
Application: M012
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2012-08-01
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: Chest Congestion 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
da6bd9df-aebe-4fe5-b20b-01bda3b9e7ee	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
49348-729-09	Chest Congestion Relief	12 in 1 BLISTER PACK	TABLET	12		4
49348-729-09	Chest Congestion Relief	2 in 1 CARTON	TABLET	2		4

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
49348-729-09	EA - Each	49348-729	4a0d884e-20ba-4609-b8ff-cd2a43c7ba68	1	2014-05-02

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
Guaifenesin	ACTIVE INGREDIENT	495W7451VQ	CHEST CONGESTION RELIEF (GUAIFENESIN) TABLET [MCKESSON]	1
Guaifenesin	ACTIVE MOIETY	495W7451VQ	CHEST CONGESTION RELIEF (GUAIFENESIN) TABLET [MCKESSON]	1
COPOVIDONE	INACTIVE INGREDIENT	D9C330MD8B	CHEST CONGESTION RELIEF (GUAIFENESIN) TABLET [MCKESSON]	1
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	CHEST CONGESTION RELIEF (GUAIFENESIN) TABLET [MCKESSON]	1
MALTODEXTRIN	INACTIVE INGREDIENT	7CVR7L4A2D	CHEST CONGESTION RELIEF (GUAIFENESIN) TABLET [MCKESSON]	1
SILICON DIOXIDE	INACTIVE INGREDIENT	ETJ7Z6XBU4	CHEST CONGESTION RELIEF (GUAIFENESIN) TABLET [MCKESSON]	1
STEARIC ACID	INACTIVE INGREDIENT	4ELV7Z65AP	CHEST CONGESTION RELIEF (GUAIFENESIN) TABLET [MCKESSON]	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
49348-729	CHEST CONGESTION RELIEF (GUAIFENESIN) TABLET [STRATEGIC SOURCING SERVICES LLC]	4	Current NDC, Legacy NDC, 2 package rows	20241220_da6bd9df-aebe-4fe5-b20b-01bda3b9e7ee.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 100 of 180 · 3,583 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Freegells Cough Drops Menthol 80ct	MENTHOL	RL Albert & Son Inc.	c96cc162-5908-4990-9dc1-3ce912844274	2025-10-08	Warnings	Exact identifier application number: M012
Freegells Cough Drops Menthol Cherry 30ct	MENTHOL	R.L. ALBERT & SON, INC	bac77712-6197-4b30-a5f8-9b99eb9d7b5a	2025-10-08	Warnings	Exact identifier application number: M012
Freegells Cough Drops Menthol Cherry 80ct	MENTHOL	R.L. ALBERT & SON, INC	6842d766-ade6-40b2-831b-f4feac25c6db	2025-10-08	Warnings	Exact identifier application number: M012
Freegells Cough Drops Menthol Cherry 80ct	MENTHOL	RL Albert & Son Inc.	9f324ca1-0e2a-47e3-997e-2aaa68a85751	2025-10-08	Warnings	Exact identifier application number: M012
Freegells Cough Drops Menthol Honey Lemon 30ct	MENTHOL	R.L. ALBERT & SON, INC	2063a013-aa0b-465d-b04f-cfe2e70d749f	2025-10-08	Warnings	Exact identifier application number: M012
Freegells Cough Drops Menthol Honey Lemon 200ct	MENTHOL	R.L. ALBERT & SON, INC	cd81488c-74d8-48d9-9c73-ff662a5cd4cd	2025-10-08	Warnings	Exact identifier application number: M012
Freegells Cough Drops Menthol Honey Lemon 80ct	MENTHOL	R.L. ALBERT & SON, INC	61deea94-d0a9-4563-926b-53f255a7c425	2025-10-08	Warnings	Exact identifier application number: M012
FREEGELLS COUGH DROPS MENTHOL STRAWBERRY 30 DROPS	MENTHOL	R.L. ALBERT & SON, INC	c6b36350-386b-4346-bef0-a37ec11319c0	2025-10-08	Warnings	Exact identifier application number: M012
Pain Reliever PM Extra Strength	ACETAMINOPHEN, DIPHENHYDRAMINE HCL	Strategic Sourcing Services LLC	3314b174-d5bb-4843-9288-9b9c5fce79d5	2025-10-08	Warnings	Exact identifier application number: M012
Allergy Relief	DIPHENHYDRAMINE HCL	CVS Pharmacy	22f55699-4922-4c05-bdf5-5844c7dd3ee5	2025-10-07	Warnings	Exact identifier application number: M012
OneSsip Diphenhydramine HCl 12.5 mg/ 5 mL Oral Solution	DIPHENHYDRAMINE HCL	MEDWISE LIFESCIENCES INC.	407b7cbb-7ebd-7b7e-e063-6394a90af501	2025-10-06	Warnings	Exact identifier application number: M012
Quality Choice Medicated Chest Rub	CAMPHOR, MENTHOL, EUCALYPTUS OIL	Quality Choice (CHAIN DRUG MARKETING ASSOCIATION)	d0cce0a0-a6bc-4c45-b9c6-08865b61c1dc	2025-10-06	Warnings	Exact identifier application number: M012
Halls Sugar Free Honey Lemon	MENTHOL	Mondelez Global LLC	2b19fdd2-8088-47f2-be20-f220a6b825fc	2025-10-06	Warnings	Exact identifier application number: M012
Giltuss Childrens Cough and Chest Congestion	DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN	Dextrum Laboratories, Inc	40802fb6-c1ec-d7b0-e063-6394a90ab423	2025-10-06	Warnings	Exact identifier application number: M012
Giltuss Diabetic	DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN	Dextrum Laboratories, Inc	3f64c81a-bbfc-4575-e063-6294a90a6ed7	2025-10-06	Warnings	Exact identifier application number: M012
TexaClear Severe Cough, Cold and Flu	CHOLINE SALICYLATE, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN	GM Pharmaceuticals, INC	cb99e5b3-1908-43c9-b31f-d35e7ce58b44	2025-10-06	Warnings	Exact identifier application number: M012
RoboHBr Cough SUPPRESSANT	DEXTROMETHORPHAN HBR	DXM Pharmaceutical, Inc	0af624ce-191f-45e1-882b-e8acb90cc77b	2025-10-06	Warnings	Exact identifier application number: M012
RoboTablets	DEXTROMETHORPHAN	DXM Pharmaceutical, Inc	b92cf698-032d-4d8d-b19c-456c6338b094	2025-10-06	Warnings	Exact identifier application number: M012
SinuLief	LORATADINE	RoseWell Pharmaceuticals LLC	32619143-a782-3497-e063-6394a90aaaec	2025-10-06	Warnings	Exact identifier application number: M012
STAHIST AD	CHLORCYCLIZINE HYDROCHLORIDE AND PSEUDOEPHEDRINE HYDROCHLORIDE	Magna Pharmaceuticals, Inc.	ccedbc38-2479-4c35-9f86-a9f29bcfab3f	2025-10-03	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	da6bd9df-aebe-4fe5-b20b-01bda3b9e7ee	4
359601	guaifenesin 400 MG Oral Tablet	SCD	da6bd9df-aebe-4fe5-b20b-01bda3b9e7ee	4

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
49348-729-09	49348072909	2 BLISTER PACK in 1 CARTON (49348-729-09) / 12 TABLET in 1 BLISTER PACK	2 blister pack	2019-08-29	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Drug Facts	Strategic Sourcing Services LLC \| Reese Pharmaceutical Co \| Pharbest	2024-12-18	HUMAN OTC DRUG LABEL	4