Pharbinex-DM

Product NDC: 73057-381
11-digit product format: 730570381
Labeler code: 73057
Product ID: 73057-381_2c2a50d1-d024-3c0f-e063-6394a90a13cc
Type: HUMAN OTC DRUG
Nonproprietary name: Guaifenesin 400mg and Dextromethorphan HBr 20mg
Dosage form: TABLET
Route: ORAL
Labeler: Ulai Health LLC
Application: M012
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2019-07-18
Substance: GUAIFENESIN; DEXTROMETHORPHAN HYDROBROMIDE
Active strength: 400; 20 mg/1; mg/1
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: 2026-12-31
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 · 4 matching rows.

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

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Package NDC	Snapshot	Source SHA-256
2025-01-20 13:05 UTC · source 2025-01-20	excluded product	product		`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	73057-381-04	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded product	product		`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	73057-381-04	`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: Pharbinex-DM
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
GUAIFENESIN	400 mg/1
DEXTROMETHORPHAN HYDROBROMIDE	20 mg/1

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
1147685	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
af80d10e-3fb2-405a-a803-1f876b8dcd10	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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
73057-381-04	2022-01-31	C162847	48780-1	d6a99b39-5068-a426-e053-dadaa90af4c2	Drug Facts
73057-381-04	2022-01-28	C162847	48780-1	d6a99b39-5068-a426-e053-dadaa90af4c2	Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
73057-381-04	Pharbinex-DM	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
73057-381	PHARBINEX-DM (GUAIFENESIN 400MG AND DEXTROMETHORPHAN HBR 20MG) TABLET [ULAI HEALTH LLC]	3	Current NDC, Legacy NDC, 1 package rows	20250122_af80d10e-3fb2-405a-a803-1f876b8dcd10.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 123 of 178 · 3,551 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
daytime cold and flu nighttime cold and flu	ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE, DOXYLAMINE SUCCINATE	Meijer, Inc.	df31056b-d0eb-4094-98d9-3d444210d50d	2025-01-16	Warnings	Exact identifier application number: M012
Childrens Ibuprofen Oral Suspension	IBUPROFEN	Reliable 1 Laboratories LLC	28dd9baa-43bd-b60a-e063-6394a90a8cf7	2025-01-15	Warnings	Exact identifier application number: M012
Guaifenesin	GUAIFENESIN	Reliable 1 Laboratories LLC	ae469d4f-91c4-cff0-e053-2995a90a0497	2025-01-15	Warnings	Exact identifier application number: M012
Diphenhydramine HCL 25 mg	DIPHENHYDRAMINE HCL	Reliable 1 Laboratories LLC	32f58cb3-941f-263b-e054-00144ff8d46c	2025-01-15	Warnings	Exact identifier application number: M012
Diphenhydramine HCl 25 mg	DIPHENHYDRAMINE HCL	Reliable 1 Laboratories LLC	32fa40ad-fed5-586f-e054-00144ff88e88	2025-01-15	Warnings	Exact identifier application number: M012
CVS Health Chest Congestion and Cough HBP SOFTGEL	DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN	CVS Pharmacy, Inc	2741ba44-1cc7-1812-e063-6394a90a8faa	2025-01-14	Warnings	Exact identifier application number: M012
DAY COLD AND FLU	ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL	TARGET CORPORATION	2b941963-8a8c-4148-e063-6294a90a1dfb	2025-01-13	Warnings	Exact identifier application number: M012
Diphenhydramine HCL	DIPHENHYDRAMINE HCL	SDA Laboratories, Inc.	437e6a13-a4ff-4f98-8973-042f224ee85e	2025-01-13	Warnings	Exact identifier application number: M012
Diphenhydramine HCL	DIPHENHYDRAMINE HCL	SDA Laboratories, Inc.	6a520986-1004-4ee6-9a47-1dfd90bb1b2c	2025-01-13	Warnings	Exact identifier application number: M012
good sense daytime	ACETAMINOPHEN, DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCL	L. Perrigo Company	5ddf3283-94e4-465d-842a-471ee946c330	2025-01-10	Warnings	Exact identifier application number: M012
Vicks VapoSteam	CAMPHOR (SYNTHETIC)	Kaz USA, Inc	c28da455-07ad-4053-8b9e-fc559f9a3f72	2025-01-10	Warnings	Exact identifier application number: M012
Guaifenesin 200mg	GUAIFENESIN	Aphena Pharma Solutions - Tennessee, LLC	45ac210a-8c54-4469-8e10-e6fe52b89cb5	2025-01-09	Warnings	Exact identifier application number: M012
Meclizine HCL	MECLIZINE HCL 25MG CHEWABLE TABLETS	Aphena Pharma Solutions - Tennessee, LLC	02d1af4d-d97d-4019-a5bf-3ec391238676	2025-01-09	Warnings	Exact identifier application number: M012
HISTEX PD Drops New Formulation	TRIPROLIDINE HYDROCHLORIDE	Allegis Pharmaceuticals, LLC	0c693f15-5d76-3dbf-e063-6294a90af9ac	2025-01-08	Warnings	Exact identifier application number: M012
DEXTROMETHORPHAN HBR 15 MG	DEXTROMETHORPHAN HBR 15 MG	AMZ789 LLC	e2175017-6a0d-0155-e053-2995a90a65d6	2025-01-08	Warnings	Exact identifier application number: M012
Nighttime Cold and Flu	ACETAMINOPHEN, DOXYLAMINE SUCCINATE, DEXTROMETHORPHAN HBR	Health Pharma USA LLC	29bb7822-76c6-e39d-e063-6294a90a64fb	2025-01-07	Warnings	Exact identifier application number: M012
Childrens Allergy Relief	CHILDRENS ALLERGY RELIEF	Allegiant Health	cb6df361-b8e5-4e2f-945f-c20159d76c4f	2025-01-06	Warnings	Exact identifier application number: M012
Nasal Decongestant PE Maximum Strength	PHENYLEPHRINE HCL	WinCo Foods, LLC	bb7a9fed-dc04-4c31-aa7f-4185d955242c	2025-01-06	Warnings	Exact identifier application number: M012
Leader Childrens Cold and Cough	BROMPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE	Cardinal Health 110, LLC. dba Leader	207b2677-aaad-4fe4-a96d-963b7dcfba70	2025-01-06	Warnings	Exact identifier application number: M012
Allergy Relief Caplet	DIPHENHYDRAMINE HYDROCHLORIDE	TOPCO ASSOCIATES LLC	126c05e7-2cd9-47d3-96c3-82305714e1db	2025-01-02	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
1147685	dextromethorphan HBr 20 MG / guaiFENesin 400 MG Oral Tablet	PSN	af80d10e-3fb2-405a-a803-1f876b8dcd10	3
1147685	dextromethorphan hydrobromide 20 MG / guaifenesin 400 MG Oral Tablet	SCD	af80d10e-3fb2-405a-a803-1f876b8dcd10	3
1147685	guaifenesin 400 MG / dextromethorphan HBr 20 MG Oral Tablet	SY	af80d10e-3fb2-405a-a803-1f876b8dcd10	3

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
73057-381-04	73057038104	30 TABLET in 1 BOTTLE, PLASTIC (73057-381-04)	30 tablet	2019-07-18	0000-00-00	No	No	Current