Cough Relief

Product NDC: 55910-309
11-digit product format: 559100309
Labeler code: 55910
Product ID: 55910-309_de92fd31-93b0-48c8-8993-8a27da244f6f
Type: HUMAN OTC DRUG
Nonproprietary name: Dextromethorphan HBr
Dosage form: LIQUID
Route: ORAL
Labeler: Dolgencorp, Inc. (DOLLAR GENERAL & REXALL)
Application: M012
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2015-08-31
Substance: DEXTROMETHORPHAN HYDROBROMIDE
Active strength: 15 mg/5mL
Pharmacologic classes: Sigma-1 Agonist [EPC], Sigma-1 Receptor Agonists [MoA], Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC], Uncompetitive NMDA Receptor Antagonists [MoA]
NDC exclude flag: No
Listing certified through: 2027-12-31
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: Cough Relief
Brand name suffix: Adult
Listing expiration: 2027-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
DEXTROMETHORPHAN HYDROBROMIDE	15 mg/5mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
9D2RTI9KYH	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
1090496	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
f5c57b32-69cb-469e-ad2d-64c00b5e66dc	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
55910-309-04	Cough ReliefAdult	118 mL in 1 BOTTLE, PLASTIC	LIQUID	118		5
55910-309-04	Cough ReliefAdult	1 in 1 BOX	LIQUID	1		5

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
DEXTROMETHORPHAN HYDROBROMIDE	ACTIVE INGREDIENT	9D2RTI9KYH	COUGH RELIEF ADULT (DEXTROMETHORPHAN HBR) LIQUID [DOLGENCORP, INC. (DOLLAR GENERAL & REXALL)]	1
DEXTROMETHORPHAN	ACTIVE MOIETY	7355X3ROTS	COUGH RELIEF ADULT (DEXTROMETHORPHAN HBR) LIQUID [DOLGENCORP, INC. (DOLLAR GENERAL & REXALL)]	1
ANHYDROUS CITRIC ACID	INACTIVE INGREDIENT	XF417D3PSL	COUGH RELIEF ADULT (DEXTROMETHORPHAN HBR) LIQUID [DOLGENCORP, INC. (DOLLAR GENERAL & REXALL)]	1
EDETATE DISODIUM	INACTIVE INGREDIENT	7FLD91C86K	COUGH RELIEF ADULT (DEXTROMETHORPHAN HBR) LIQUID [DOLGENCORP, INC. (DOLLAR GENERAL & REXALL)]	1
FD&C YELLOW NO. 6	INACTIVE INGREDIENT	H77VEI93A8	COUGH RELIEF ADULT (DEXTROMETHORPHAN HBR) LIQUID [DOLGENCORP, INC. (DOLLAR GENERAL & REXALL)]	1
GLYCERIN	INACTIVE INGREDIENT	PDC6A3C0OX	COUGH RELIEF ADULT (DEXTROMETHORPHAN HBR) LIQUID [DOLGENCORP, INC. (DOLLAR GENERAL & REXALL)]	1
HIGH FRUCTOSE CORN SYRUP	INACTIVE INGREDIENT	XY6UN3QB6S	COUGH RELIEF ADULT (DEXTROMETHORPHAN HBR) LIQUID [DOLGENCORP, INC. (DOLLAR GENERAL & REXALL)]	1
HYDROXYETHYL CELLULOSE (1500 MPA.S AT 1%)	INACTIVE INGREDIENT	L605B5892V	COUGH RELIEF ADULT (DEXTROMETHORPHAN HBR) LIQUID [DOLGENCORP, INC. (DOLLAR GENERAL & REXALL)]	1
POLYETHYLENE GLYCOLS	INACTIVE INGREDIENT	3WJQ0SDW1A	COUGH RELIEF ADULT (DEXTROMETHORPHAN HBR) LIQUID [DOLGENCORP, INC. (DOLLAR GENERAL & REXALL)]	1
PROPYLENE GLYCOL	INACTIVE INGREDIENT	6DC9Q167V3	COUGH RELIEF ADULT (DEXTROMETHORPHAN HBR) LIQUID [DOLGENCORP, INC. (DOLLAR GENERAL & REXALL)]	1
SODIUM BENZOATE	INACTIVE INGREDIENT	OJ245FE5EU	COUGH RELIEF ADULT (DEXTROMETHORPHAN HBR) LIQUID [DOLGENCORP, INC. (DOLLAR GENERAL & REXALL)]	1
SUCRALOSE	INACTIVE INGREDIENT	96K6UQ3ZD4	COUGH RELIEF ADULT (DEXTROMETHORPHAN HBR) LIQUID [DOLGENCORP, INC. (DOLLAR GENERAL & REXALL)]	1
SUCROSE	INACTIVE INGREDIENT	C151H8M554	COUGH RELIEF ADULT (DEXTROMETHORPHAN HBR) LIQUID [DOLGENCORP, INC. (DOLLAR GENERAL & REXALL)]	1
WATER	INACTIVE INGREDIENT	059QF0KO0R	COUGH RELIEF ADULT (DEXTROMETHORPHAN HBR) LIQUID [DOLGENCORP, INC. (DOLLAR GENERAL & REXALL)]	1
XANTHAN GUM	INACTIVE INGREDIENT	TTV12P4NEE	COUGH RELIEF ADULT (DEXTROMETHORPHAN HBR) LIQUID [DOLGENCORP, INC. (DOLLAR GENERAL & REXALL)]	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
55910-309	COUGH RELIEF ADULT (DEXTROMETHORPHAN HBR) LIQUID [DOLGENCORP, INC. (DOLLAR GENERAL & REXALL)]	5	Current NDC, Legacy NDC, 2 package rows	20241016_f5c57b32-69cb-469e-ad2d-64c00b5e66dc.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 132 of 180 · 3,583 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
DUAL ACTION CHERRY COUGH SUPPRESSANT ORAL ANESTHETIC	MENTHOL	Ricola USA Inc.	82813342-2be2-4731-ae90-dbd5eed667a9	2024-12-10	Warnings	Exact identifier application number: M012
MOUNTAIN HERB SUGAR FREE WITH STEVIA COUGH SUPPRESSANT ORAL ANESTHETIC	MENTHOL	Ricola USA Inc.	b640a5d2-a7fe-486d-a65f-e7c993f950d6	2024-12-10	Warnings	Exact identifier application number: M012
Sugar Free Mountain Herb Cough Suppressant Throat Drops	MENTHOL	Ricola USA Inc.	c3f3c062-55e5-43c1-a016-ee47a7b388a5	2024-12-10	Warnings	Exact identifier application number: M012
RICOLA MAX THROAT CARE SWISS CHERRY	MENTHOL	Ricola USA Inc.	ee4733b5-6e5a-438a-97da-110f3ef6c809	2024-12-10	Warnings	Exact identifier application number: M012
SUGAR FREE GREEN TEA WITH ECHINACEA COUGH SUPPRESSANT THROAT DROPS	MENTHOL	Ricola USA Inc.	f62fcc38-2d43-40b3-841f-c8eea9ebd1e1	2024-12-10	Warnings	Exact identifier application number: M012
DUAL ACTION HONEY LEMON COUGH SUPPRESSANT ORAL ANESTHETIC	MENTHOL	Ricola USA Inc.	8a6db093-7e52-443f-8dd6-94867606fef8	2024-12-10	Warnings	Exact identifier application number: M012
RICOLA MAX THROAT CARE COOL PEPPERMINT	MENTHOL	Ricola USA Inc.	5885343e-4a6e-44f7-87a4-d52599156197	2024-12-10	Warnings	Exact identifier application number: M012
EXTRA STRENGTH WITH NATURAL MENTHOL GLACIER MINT COUGH SUPPRESSANT	MENTHOL	Ricola USA Inc.	0baf383c-886d-47ca-8a6d-221298c79446	2024-12-10	Warnings	Exact identifier application number: M012
Tussin Multi Symptom Cold CF	DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE	Best Choice (Valu Merchandisers Company)	539b8972-2a46-468e-ad27-6672d746feb7	2024-12-10	Warnings	Exact identifier application number: M012
DUAL ACTION GLACIER MINT COUGH SUPPRESSANT ORAL ANESTHETIC	MENTHOL	Ricola USA Inc.	db2ab9be-507d-4768-9d00-188f751b7726	2024-12-10	Warnings	Exact identifier application number: M012
Adult Allergy Relief	CALMCO ALLERGY RELIEF	CalmCo	08288825-0f38-b6a3-e063-6394a90aa358	2024-12-07	Warnings	Exact identifier application number: M012
Original Herb Cough Drops	MENTHOL	Ricola Ag	c142663f-086e-4ab7-a758-9107d7077537	2024-12-05	Warnings	Exact identifier application number: M012
DUAL ACTION CHERRY COUGH SUPPRESSANT ORAL ANESTHETIC	MENTHOL	Ricola Ag	984c9793-163c-4b97-b244-9b471966a122	2024-12-05	Warnings	Exact identifier application number: M012
BENZEDREX	PROPYLHEXEDRINE	BF ASCHER AND CO INC	00d8c237-3eee-1d9f-e063-6394a90aeb86	2024-12-05	Warnings	Exact identifier application number: M012
Cold Multi Symptom Daytime Nighttime	ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE, AND PHENYLEPHRINE HYDROCHLORIDE	Chain Drug Marketing Association	d5cbb5b0-564c-429e-b680-fa683e796393	2024-12-05	Warnings	Exact identifier application number: M012
Cold Relief Multi-Symptom	ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE, AND PHENYLEPHRINE HYDROCHLORIDE	TopCare	de8a623f-7b10-4d56-a74b-3737e7716ffe	2024-12-05	Warnings	Exact identifier application number: M012
Cold Max Daytime	ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, AND PHENYLEPHRINE HYDROCHLORIDE	TopCo Associates LLC	9773958b-c5e5-4da7-a8e9-6b6c223a2b30	2024-12-05	Warnings	Exact identifier application number: M012
Cold Plus Head Congestion Daytime	ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, AND PHENYLEPHRINE HYDROCHLORIDE	TopCo Associates LLC	399e0e51-c2a7-451c-b74d-d3db140cef69	2024-12-05	Warnings	Exact identifier application number: M012
Head Congestion Plus Mucus PE	ACETAMINOPHEN, GUAIFENESIN, AND PHENYLEPHRINE HYDROCHLORIDE	United Natural Foods, Inc. dba UNFI	09531edc-8dbd-451f-ae02-f922e9e8c248	2024-12-05	Warnings	Exact identifier application number: M012
DUAL ACTION CHERRY COUGH SUPPRESSANT ORAL ANESTHETIC	MENTHOL	Ricola Ag	71ca8af7-172d-40da-be1e-ff3ab5568e74	2024-12-05	Warnings	Exact identifier application number: M012

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
9D2RTI9KYH	DEXTROMETHORPHAN HYDROBROMIDE	6700-34-1	DEXTROMETHORPHAN HYDROBROMIDE

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
1090496	dextromethorphan HBr 15 MG in 5 mL Oral Solution	PSN	f5c57b32-69cb-469e-ad2d-64c00b5e66dc	5
1090496	dextromethorphan hydrobromide 3 MG/ML Oral Solution	SCD	f5c57b32-69cb-469e-ad2d-64c00b5e66dc	5
1090496	dextromethorphan hydrobromide 15 MG per 5 ML Oral Solution	SY	f5c57b32-69cb-469e-ad2d-64c00b5e66dc	5
1090496	dextromethorphan hydrobromide 30 MG per 10 ML Oral Solution	SY	f5c57b32-69cb-469e-ad2d-64c00b5e66dc	5

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Marketing start	Marketing end	Sample	Exclude flag	Status
55910-309-04	55910030904	1 BOTTLE, PLASTIC in 1 BOX (55910-309-04) / 118 mL in 1 BOTTLE, PLASTIC	2015-08-31	0000-00-00	No	No	Current