Supress DM

Product NDC: 52083-058
11-digit product format: 520830058
Labeler code: 52083
Product ID: 52083-058_974dbf24-7689-4e94-a535-d5b59c097406
Type: HUMAN OTC DRUG
Nonproprietary name: dextromethorphan hydrobromide, guaifenesin
Dosage form: SYRUP
Route: ORAL
Labeler: KRAMER NOVIS
Application: M012
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2013-10-02
Substance: GUAIFENESIN; DEXTROMETHORPHAN HYDROBROMIDE
Active strength: 50; 5 mg/mL; mg/mL
Pharmacologic classes: Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE], 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

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 16 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Package NDC	Code	Status	Snapshot	Source SHA-256
2025-08-27 00:01 UTC · source 2025-08-26	excluded product	product		I	Inactivated by FDA	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	52083-058-01	I	Inactivated by FDA	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded product	product		I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	52083-058-01	I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded product	product		I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	52083-058-01	I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded product	product		I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	52083-058-01	I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded product	product		I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	52083-058-01	I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded product	product		U	Excluded because listing certification expired	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	52083-058-01	U	Excluded because listing certification expired	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded product	product		U	Excluded because listing certification expired	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	52083-058-01	U	Excluded because listing certification expired	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded product	product		U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	52083-058-01	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`

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: Supress DM
Listing expiration: 2027-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
GUAIFENESIN	50 mg/mL
DEXTROMETHORPHAN HYDROBROMIDE	5 mg/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
495W7451VQ	Internal UNII lookup
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
1439992	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
7da0611e-729c-4cf8-88f3-f8877b9f5cfa	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
bf324df6-7127-7deb-def5-2681c136cd03	Product name	3	20250325
43a1ed49-eae2-4840-8075-cb4b33478540	Product name	1	20230425
ba088a92-ab5e-b2d4-e908-f5ea691b7587	Product name	7	20210201
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
76633df9-0d59-4b88-03ed-21dee1b966f8	Product name	1	20140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
52083-058-01	2025-11-18	C162847	48780-1	2cef2736-5f9c-d83d-e063-dadaa90ab31f	Supress DM
52083-058-01	2025-01-30	C162847	48780-1	2cef2736-5f9c-d83d-e063-dadaa90ab31f	Supress DM

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
52083-058-01	Supress DM	30 mL in 1 BOTTLE	SYRUP	30		5

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
52083-058-01	ML - Milliliter	52083-058	9db1418f-5f10-40ad-9fa8-1f0b9c5e8a85	1	2013-12-02

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
DEXTROMETHORPHAN HYDROBROMIDE	ACTIVE INGREDIENT	9D2RTI9KYH	SUPRESS DM (DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN) SYRUP [KRAMER NOVIS]	1
GUAIFENESIN	ACTIVE INGREDIENT	495W7451VQ	SUPRESS DM (DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN) SYRUP [KRAMER NOVIS]	1
DEXTROMETHORPHAN	ACTIVE MOIETY	7355X3ROTS	SUPRESS DM (DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN) SYRUP [KRAMER NOVIS]	1
GUAIFENESIN	ACTIVE MOIETY	495W7451VQ	SUPRESS DM (DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN) SYRUP [KRAMER NOVIS]	1
CITRIC ACID MONOHYDRATE	INACTIVE INGREDIENT	2968PHW8QP	SUPRESS DM (DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN) SYRUP [KRAMER NOVIS]	1
GLYCERIN	INACTIVE INGREDIENT	PDC6A3C0OX	SUPRESS DM (DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN) SYRUP [KRAMER NOVIS]	1
METHYLPARABEN	INACTIVE INGREDIENT	A2I8C7HI9T	SUPRESS DM (DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN) SYRUP [KRAMER NOVIS]	1
PROPYLENE GLYCOL	INACTIVE INGREDIENT	6DC9Q167V3	SUPRESS DM (DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN) SYRUP [KRAMER NOVIS]	1
PROPYLPARABEN	INACTIVE INGREDIENT	Z8IX2SC1OH	SUPRESS DM (DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN) SYRUP [KRAMER NOVIS]	1
SACCHARIN SODIUM	INACTIVE INGREDIENT	SB8ZUX40TY	SUPRESS DM (DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN) SYRUP [KRAMER NOVIS]	1
SODIUM CITRATE	INACTIVE INGREDIENT	1Q73Q2JULR	SUPRESS DM (DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN) SYRUP [KRAMER NOVIS]	1
WATER	INACTIVE INGREDIENT	059QF0KO0R	SUPRESS DM (DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN) SYRUP [KRAMER NOVIS]	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
52083-058	SUPRESS DM (DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN) SYRUP [KRAMER NOVIS]	4	Current NDC, Legacy NDC, 1 package rows	20181213_7da0611e-729c-4cf8-88f3-f8877b9f5cfa.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 150 of 178 · 3,551 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Tukol Cough and Congestion	DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, AND PHENYLEPHRINE HYDROCHLORIDE	Genomma Lab USA	27ab3d86-e960-4d83-aad1-d50d2c8e02a9	2024-10-14	Warnings	Exact identifier application number: M012
HealthWise Chest Rub Lavender	CAMPHOR, MENTHOL, EUCALYPTUS OIL	Veridian Healthcare	2472ce85-c701-4fcd-e063-6394a90a2765	2024-10-14	Warnings	Exact identifier application number: M012
HealthWise Chest Rub Lemon	CAMPHOR, MENTHOL, EUCALYPTUS OIL	Veridian Healthcare	24740d5a-aba1-0bd4-e063-6394a90ab2ca	2024-10-14	Warnings	Exact identifier application number: M012
Childrens Plus Cough and Runny Nose	ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE	Dolgencorp, Inc. (DOLLAR GENERAL & REXALL)	ea059b56-dc9a-4a6b-8c16-5dfcdaf4cd43	2024-10-14	Warnings	Exact identifier application number: M012
Theraflu Severe Cold Relief	ACETAMINOPHEN, DEXTROMETHORPHAN HBR, DIPHENPHYDRAMINE HCL, GUAIFENESIN	Haleon US Holdings LLC	b01cc9f5-53f2-40d8-acf1-6de180b3d0bf	2024-10-14	Warnings	Exact identifier application number: M012
Cough Relief Adult	DEXTROMETHORPHAN HBR	Dolgencorp, Inc. (DOLLAR GENERAL & REXALL)	f5c57b32-69cb-469e-ad2d-64c00b5e66dc	2024-10-14	Warnings	Exact identifier application number: M012
Nasal Decongestant	PSEUDOEPHEDRINE HCL	Publix Super Markets Inc	94c21df5-c631-4748-a833-288b2298055c	2024-10-12	Warnings	Exact identifier application number: M012
Allergy Relief	DIPHENHYDRAMINE HYDROCHLORIDE	Chain Drug Marketing Association	8eab9d79-69c1-44b8-9145-a7ebd887d54d	2024-10-11	Warnings	Exact identifier application number: M012
Allergy Relief	DIPHENHYDRAMINE HYDROCHLORIDE	Chain Drug Marketing Association	e4963eec-fb4a-425c-be19-f514b4f10a7f	2024-10-11	Warnings	Exact identifier application number: M012
Severe Sinus Congestion and Pain	ACETAMINOPHEN, GUAIFENESIN, AND PHENYLEPHRINE HYDROCHLORIDE	Chain Drug Marketing Association	1b4e87f8-3f9e-4865-9128-527d2d621593	2024-10-11	Warnings	Exact identifier application number: M012
Mucus Relief Cold and Flu All in One	ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, AND PHENYLEPHRINE HYDROCHLORIDE	CHAIN DRUG MARKETING ASSOCIATION INC	ff433512-55b7-4fc9-8a55-aff5cbb749ef	2024-10-11	Warnings	Exact identifier application number: M012
Mucus Relief Cold Flu and Sore Throat	ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, AND PHENYLEPHRINE HYDROCHLORIDE	CHAIN DRUG MARKETING ASSOCIATION INC	3170354a-4752-49a0-97ed-3d9db266a059	2024-10-11	Warnings	Exact identifier application number: M012
Tukol Children Cough and Congestion	DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, AND PHENYLEPHRINE HYDROCHLORIDE	Genomma Lab USA	235a6d2b-7302-410c-be35-4d5ff7bbdfce	2024-10-11	Warnings	Exact identifier application number: M012
Night Time Cold and Flu Relief Multi Symptom	ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE	CVS Pharmacy	6c7b0ea6-bff9-4fd2-9e00-64015c326ee8	2024-10-11	Warnings	Exact identifier application number: M012
nitetime cold and flu	ACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATE	Meijer Distribution Inc	dcc12bc2-4bb4-4d2d-8206-b9db9843ec8b	2024-10-11	Warnings	Exact identifier application number: M012
Signature Care Nasal Decongestant	OXYMETAZOLINE HYDROCHLORIDE	Safeway	838d2f11-2ee4-4081-98c8-b87e79aa47c4	2024-10-11	Warnings	Exact identifier application number: M012
Menthol	COUGH SUPPRESSANT	McKesson	9d4def70-480f-f2fa-e053-2995a90a9877	2024-10-10	Warnings	Exact identifier application number: M012
Menthol	COUGH SUPPRESSANT	McKesson	9d5b4ef6-4eb8-41f6-e053-2a95a90a1350	2024-10-10	Warnings	Exact identifier application number: M012
Tukol Sugar Free Cough and Cold	DEXTROMETHORPHAN HYDROBROMIDE AND GUAIFENESIN	Genomma Lab USA	95e0a3eb-5a58-4c8b-a70b-fb0cca1e0841	2024-10-08	Warnings	Exact identifier application number: M012
Rompe Pecho CF CF	BROMPHENIRAMINE MALEATE, DEXTROMETHORPHAN HBR	Efficient Laboratories Inc	06e96e0c-f21f-e706-e063-6294a90a0780	2024-10-08	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
9D2RTI9KYH	DEXTROMETHORPHAN HYDROBROMIDE	6700-34-1	DEXTROMETHORPHAN HYDROBROMIDE

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
1439992	dextromethorphan HBr 5 MG / guaiFENesin 50 MG in 1 mL Oral Solution	PSN	7da0611e-729c-4cf8-88f3-f8877b9f5cfa	5
1439992	dextromethorphan hydrobromide 5 MG/ML / guaifenesin 50 MG/ML Oral Solution	SCD	7da0611e-729c-4cf8-88f3-f8877b9f5cfa	5
1439992	dextromethorphan hydrobromide 5 MG/ML / GG 50 MG/ML Oral Solution	SY	7da0611e-729c-4cf8-88f3-f8877b9f5cfa	5

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
52083-058-01	52083005801	30 mL in 1 BOTTLE (52083-058-01)	30 ml	2013-10-02	0000-00-00	No	No	Current