DG Health Immediate Release Mucus Relief

Product NDC: 10956-059
11-digit product format: 109560059
Labeler code: 10956
Product ID: 10956-059_1938e502-ee72-400d-933c-271efa88dc69
Type: HUMAN OTC DRUG
Nonproprietary name: Guaifenesin
Dosage form: TABLET
Route: ORAL
Labeler: Reese Pharmaceutical Co
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

Additional Listing Data#

Finished product: Yes
Brand name base: DG Health Immediate Release 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
f60a9d1b-7a63-43d3-b843-e1f31cf78873	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
10956-059-30	DG Health Immediate Release Mucus Relief	1 in 1 CARTON	TABLET	1		3
10956-059-30	DG Health Immediate Release Mucus Relief	30 in 1 BOTTLE, PLASTIC	TABLET	30		3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
10956-059	DG HEALTH IMMEDIATE RELEASE MUCUS RELIEF (GUAIFENESIN) TABLET [REESE PHARMACEUTICAL CO]	3	Current NDC, Legacy NDC, 2 package rows	20241220_f60a9d1b-7a63-43d3-b843-e1f31cf78873.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 99 of 196 · 3,909 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Meijer Childrens Allergy Relief Bubblegum flavor	DIPHENHYDRAMINE HCL	MEIJER DISTRIBUTION INC	d3f7b0ee-51e8-466f-ad9f-98ac879c330a	2025-10-24	Warnings	Exact identifier application number: M012
Meijer Original	NASAL	MEIJER DISTRIBUTION INC	61d7db6f-1180-4ed5-9ad4-c98b3964536b	2025-10-24	Warnings	Exact identifier application number: M012
Meijer Maximum Strength Severe Congestion and Cough	DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, AND PHENYLEPHRINE HYDROCHLORIDE	MEIJER, INC.	5d2b54e5-1cb7-4071-9de2-afae33536c49	2025-10-24	Warnings	Exact identifier application number: M012
Meijer Mucus Relief DM Maximum Strength	DEXTROMETHORPHAN HBR AND GUAIFENESIN	MEIJER, INC.	12cbe71a-a796-4f14-848e-aa6082dac032	2025-10-24	Warnings	Exact identifier application number: M012
Meijer Adult Mucus Plus chest congestion	GUAIFENESIN	MEIJER DISTRIBUTION, INC	f6a23be6-0313-4c23-afb7-576666b80e21	2025-10-24	Warnings	Exact identifier application number: M012
Meijer Children Cough and Chest Congestion DM Grape Flavor	DEXTROMETHORPHAN HBR AND GUAIFENESIN	MEIJER DISTRIBUTION INC	9121804a-e5eb-46a2-a4a7-cc625be846d1	2025-10-24	Warnings	Exact identifier application number: M012
meijer Maximum Strength Nighttime Cough DM	DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE	MEIJER DISTRIBUTION INC	a99f36b1-6cf4-496e-a347-08aa21cba163	2025-10-24	Warnings	Exact identifier application number: M012
Maximum Strength Mucus Relief Severe Congestion and Cough Cooling Menthol	DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, AND PHENYLEPHRINE HYDROCHLORIDE	MEIJER DISTRIBUTION INC	ab8322f6-8474-4043-8f2b-a71e3f3b48ce	2025-10-24	Warnings	Exact identifier application number: M012
Daytime Nighttime Severe Cold and Flu Relief	ACETAMINOPHEN DEXTROMETHORPHAN HBR GUAIFENESIN PHENYLEPHRINE HCI DOXYLAMINE SUCINATE	Family Dollar (FAMILY WELLNESS)	22918db6-9096-4eb8-a742-aaa2dd5c31da	2025-10-24	Warnings	Exact identifier application number: M012
Daytime Sinus Severe	ACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HCL	Kroger Company	1022767d-a456-4fbc-95cf-91337c74c330	2025-10-24	Warnings	Exact identifier application number: M012
Daytime Severe Cold and Flu Relief	ACETAMINOPHEN DEXTROMETHORPHAN HBR GUAIFENESIN, PHENYLEPHRINE HCL	Family Dollar (FAMILY WELLNESS)	17640528-c1f7-4881-ba86-bb3f488a952c	2025-10-24	Warnings	Exact identifier application number: M012
Vapor Stick	CAMPHOR/MENTHOL	China Ningbo Shangge Cosmetics Technology Corp.	33e259d6-b065-a677-e063-6394a90ab314	2025-10-23	Warnings	Exact identifier application number: M012
Severe Nighttime Severe Daytime	ACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATE, PHENYLEPHRINE HCL	CVS Pharmacy	1ec3fc79-4f38-439f-99be-646b82231aa5	2025-10-23	Warnings	Exact identifier application number: M012
daytime nighttime cold and flu	ACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATE, PHENYLEPHRINE HCL	Walgreen Company	12fd5713-0ae4-4d6a-bf33-7e3d76e10c78	2025-10-22	Warnings	Exact identifier application number: M012
allergy relief childrens	DIPHENHYDRAMINE HCL	CVS Pharmacy	8b539dc0-5487-4b11-babd-52bf341a8947	2025-10-22	Warnings	Exact identifier application number: M012
Rycontuss	CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE	Dextrum Laboratories, Inc	41afb883-1158-9764-e063-6294a90a1712	2025-10-21	Warnings	Exact identifier application number: M012
Acetaminophen, Dextromethorphan HBr, Chlorpheniramine Maleate	ACETAMINOPHEN, DEXTROMETHORPHAN HBR, CHLORPHENIRAMINE MALEATE	CVS Pharmacy, Inc	1532ee21-e114-ded7-e063-6294a90ab025	2025-10-21	Warnings	Exact identifier application number: M012
Guaifenesin and Dextromethorphan Hydrobromide	GUAIFENESIN AND DEXTROMETHORPHAN HYDROBROMIDE	Method Pharmaceuticals	1538bf63-d020-3ba2-e063-6294a90aecc5	2025-10-21	Warnings	Exact identifier application number: M012
Guaifenesin and Dextromethorphan Hydrobromide	GUAIFENESIN AND DEXTROMETHORPHAN HYDROBROMIDE	Method Pharmaceuticals	389230e5-775e-5b0d-e054-00144ff88e88	2025-10-21	Warnings	Exact identifier application number: M012
Guaifenesin	GUAIFENESIN	Method Pharmaceuticals, LLC	1539c3d4-d982-7d4e-e063-6394a90ad7d6	2025-10-21	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	f60a9d1b-7a63-43d3-b843-e1f31cf78873	3
359601	guaifenesin 400 MG Oral Tablet	SCD	f60a9d1b-7a63-43d3-b843-e1f31cf78873	3

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Marketing start	Marketing end	Sample	Exclude flag	Status
10956-059-30	10956005930	1 BOTTLE, PLASTIC in 1 CARTON (10956-059-30) / 30 TABLET in 1 BOTTLE, PLASTIC	2013-12-01	0000-00-00	No	No	Current