SUDOGEST NASAL DECONGESTANT

Product NDC
50090-4345
11-digit product format
500904345
Labeler code
50090
Product ID
50090-4345_72064c3e-8348-4230-b2e3-47a03e3467df
Type
HUMAN OTC DRUG
Nonproprietary name
Pseudoephedrine HCl
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
A-S Medication Solutions
Application
M012
Marketing category
OTC MONOGRAPH DRUG
Marketing start
1991-09-10
Substance
PSEUDOEPHEDRINE HYDROCHLORIDE
Active strength
30 mg/1
Pharmacologic classes
Adrenergic alpha-Agonists [MoA], alpha-Adrenergic Agonist [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 5 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage50090-434550090-4345-0DDiscontinued by firm2026-10-23
excluded packagepackage50090-434550090-4345-2DDiscontinued by firm2026-10-23
excluded packagepackage50090-434550090-4345-3DDiscontinued by firm2026-10-23
excluded packagepackage50090-434550090-4345-4DDiscontinued by firm2026-10-23
excluded packagepackage50090-434550090-4345-5DDiscontinued by firm2026-10-23

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 · 50 matching rows.

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

Captured / source date, Package NDC, Snapshot table
Captured / source datePackage NDCSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-0550090-4345-4d630ba8d3edf…732f749b63fb…
2025-12-14 17:58 UTC · source 2025-12-0550090-4345-3d630ba8d3edf…732f749b63fb…
2025-12-14 17:58 UTC · source 2025-12-0550090-4345-2d630ba8d3edf…732f749b63fb…
2025-12-14 17:58 UTC · source 2025-12-0550090-4345-5d630ba8d3edf…732f749b63fb…
2025-12-14 17:58 UTC · source 2025-12-0550090-4345-0d630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-2650090-4345-4f5e01cc5f278…a2eaf40c39c3…
2025-08-27 00:01 UTC · source 2025-08-2650090-4345-3f5e01cc5f278…a2eaf40c39c3…
2025-08-27 00:01 UTC · source 2025-08-2650090-4345-2f5e01cc5f278…a2eaf40c39c3…
2025-08-27 00:01 UTC · source 2025-08-2650090-4345-5f5e01cc5f278…a2eaf40c39c3…
2025-08-27 00:01 UTC · source 2025-08-2650090-4345-0f5e01cc5f278…a2eaf40c39c3…
2025-04-01 02:39 UTC · source 2025-03-3150090-4345-42ef7874e63bc…57b86245f4fa…
2025-04-01 02:39 UTC · source 2025-03-3150090-4345-32ef7874e63bc…57b86245f4fa…
2025-04-01 02:39 UTC · source 2025-03-3150090-4345-22ef7874e63bc…57b86245f4fa…
2025-04-01 02:39 UTC · source 2025-03-3150090-4345-52ef7874e63bc…57b86245f4fa…
2025-04-01 02:39 UTC · source 2025-03-3150090-4345-02ef7874e63bc…57b86245f4fa…
2025-03-28 20:22 UTC · source 2025-03-2850090-4345-4a1b67e2a42f9…c4cf2c586c0d…
2025-03-28 20:22 UTC · source 2025-03-2850090-4345-3a1b67e2a42f9…c4cf2c586c0d…
2025-03-28 20:22 UTC · source 2025-03-2850090-4345-2a1b67e2a42f9…c4cf2c586c0d…
2025-03-28 20:22 UTC · source 2025-03-2850090-4345-5a1b67e2a42f9…c4cf2c586c0d…
2025-03-28 20:22 UTC · source 2025-03-2850090-4345-0a1b67e2a42f9…c4cf2c586c0d…
2025-03-22 03:12 UTC · source 2025-03-2150090-4345-4cfe11265f3b6…090c488252e2…
2025-03-22 03:12 UTC · source 2025-03-2150090-4345-3cfe11265f3b6…090c488252e2…
2025-03-22 03:12 UTC · source 2025-03-2150090-4345-2cfe11265f3b6…090c488252e2…
2025-03-22 03:12 UTC · source 2025-03-2150090-4345-5cfe11265f3b6…090c488252e2…
2025-03-22 03:12 UTC · source 2025-03-2150090-4345-0cfe11265f3b6…090c488252e2…
2025-03-10 12:48 UTC · source 2025-03-1050090-4345-4cdf11ea48f46…ba0047e9e063…
2025-03-10 12:48 UTC · source 2025-03-1050090-4345-3cdf11ea48f46…ba0047e9e063…
2025-03-10 12:48 UTC · source 2025-03-1050090-4345-2cdf11ea48f46…ba0047e9e063…
2025-03-10 12:48 UTC · source 2025-03-1050090-4345-5cdf11ea48f46…ba0047e9e063…
2025-03-10 12:48 UTC · source 2025-03-1050090-4345-0cdf11ea48f46…ba0047e9e063…
2025-02-02 03:52 UTC · source 2025-01-3150090-4345-4302b2466d912…e7b80fea0513…
2025-02-02 03:52 UTC · source 2025-01-3150090-4345-3302b2466d912…e7b80fea0513…
2025-02-02 03:52 UTC · source 2025-01-3150090-4345-2302b2466d912…e7b80fea0513…
2025-02-02 03:52 UTC · source 2025-01-3150090-4345-5302b2466d912…e7b80fea0513…
2025-02-02 03:52 UTC · source 2025-01-3150090-4345-0302b2466d912…e7b80fea0513…
2025-01-20 13:05 UTC · source 2025-01-2050090-4345-4ed331223b511…672a5bd82f5f…
2025-01-20 13:05 UTC · source 2025-01-2050090-4345-3ed331223b511…672a5bd82f5f…
2025-01-20 13:05 UTC · source 2025-01-2050090-4345-2ed331223b511…672a5bd82f5f…
2025-01-20 13:05 UTC · source 2025-01-2050090-4345-5ed331223b511…672a5bd82f5f…
2025-01-20 13:05 UTC · source 2025-01-2050090-4345-0ed331223b511…672a5bd82f5f…
2025-01-11 03:41 UTC · source 2025-01-1050090-4345-40efc9e666f02…f202fb6c5f17…
2025-01-11 03:41 UTC · source 2025-01-1050090-4345-30efc9e666f02…f202fb6c5f17…
2025-01-11 03:41 UTC · source 2025-01-1050090-4345-20efc9e666f02…f202fb6c5f17…
2025-01-11 03:41 UTC · source 2025-01-1050090-4345-50efc9e666f02…f202fb6c5f17…
2025-01-11 03:41 UTC · source 2025-01-1050090-4345-00efc9e666f02…f202fb6c5f17…
2024-11-09 02:27 UTC · source 2024-11-0850090-4345-4ad56d346431e…cc804d4bbf1e…
2024-11-09 02:27 UTC · source 2024-11-0850090-4345-3ad56d346431e…cc804d4bbf1e…
2024-11-09 02:27 UTC · source 2024-11-0850090-4345-2ad56d346431e…cc804d4bbf1e…
2024-11-09 02:27 UTC · source 2024-11-0850090-4345-5ad56d346431e…cc804d4bbf1e…
2024-11-09 02:27 UTC · source 2024-11-0850090-4345-0ad56d346431e…cc804d4bbf1e…

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
SUDOGEST NASAL DECONGESTANT
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
PSEUDOEPHEDRINE HYDROCHLORIDE30 mg/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
6V9V2RYJ8NInternal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
1049160Internal RxNorm lookup
1049162Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
09feb5f0-c22d-4a1b-97a0-d5767e5f7730Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
ba088a92-ab5e-b2d4-e908-f5ea691b7587Product name720210201
0fdb98e2-b951-a1ce-5715-2b187ba500efProduct name420170718
e974e22d-8688-7d92-1e87-40c1079e170cProduct name320151125
e8718272-64cb-4436-969b-176c3067c8f4Product name120150609
30c51294-7ae9-8007-7de6-58222684a0beProduct name120140508
4f26f669-fc6c-40ef-9e26-1c7b2390ee66Product name120140508
70a83adc-6047-bbea-5a08-dfd304aa47d2Product name120140508
858ce051-9941-aafc-8c7c-44a8e0227463Product name120140508
b893258d-0942-3d8a-3411-056ea0788ff5Product name120140508

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
50090-4345-0SUDOGEST NASAL DECONGESTANT48 in 1 BOTTLETABLET, FILM COATED4810
50090-4345-1SUDOGEST NASAL DECONGESTANT1 in 1 BLISTER PACKTABLET, FILM COATED110
50090-4345-1SUDOGEST NASAL DECONGESTANT24 in 1 CARTONTABLET, FILM COATED2410
50090-4345-2SUDOGEST NASAL DECONGESTANT12 in 1 BOTTLETABLET, FILM COATED1210
50090-4345-3SUDOGEST NASAL DECONGESTANT30 in 1 BOTTLETABLET, FILM COATED3010
50090-4345-4SUDOGEST NASAL DECONGESTANT4 in 1 BOTTLETABLET, FILM COATED410
50090-4345-5SUDOGEST NASAL DECONGESTANT15 in 1 BOTTLETABLET, FILM COATED1510

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
50090-4345-1EA - Each50090-4345a510bcc2-0b21-485b-b9e5-434600a4917112022-09-12

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50090-4345SUDOGEST NASAL DECONGESTANT (PSEUDOEPHEDRINE HCL) TABLET, FILM COATED [A-S MEDICATION SOLUTIONS]10Current NDC, Legacy NDC, 7 package rows20241109_09feb5f0-c22d-4a1b-97a0-d5767e5f7730.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 60 of 178 · 3,550 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Alka-Seltzer Plus Severe Cold PowerFast Fizz Day and NightASPIRIN, CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE BITARTRATEBayer HealthCare LLC.fc60af2f-83cb-99ea-e053-6394a90a0b3b2026-01-08WarningsExact identifier
application number: M012
Alka Seltzer Plus Maximum Strength Sinus, Allergy And Cough Power Max GelsACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE , DOXYLAMINE SUCCINATE, PHENYLEPHRINE HYDROCHLORIDEBayer HealthCare LLC.e17eb929-209d-a2d1-e053-2a95a90a4cf32026-01-08WarningsExact identifier
application number: M012
Alka-Seltzer Plus Severe Cold Night PowerFast FizzASPIRIN, DOXYLAMINE SUCCINATE, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE BITARTRATEBayer HealthCare LLC.c1fae6c7-bbac-1320-e053-2a95a90aac5a2026-01-08WarningsExact identifier
application number: M012
Alka-Seltzer Plus Night Severe Cold and FluACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE, AND PHENYLEPHRINE HYDROCHLORIDEBayer HealthCare LLC.f4c60ca1-ba59-4a92-84a5-6ba65faa56ab2026-01-08WarningsExact identifier
application number: M012
Alka-Seltzer Plus Day Severe Cold Plus FluACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, AND PHENYLEPHRINE HYDROCHLORIDEBayer HealthCare LLC.cec51eab-cce3-4965-a14e-a46d953050c42026-01-08WarningsExact identifier
application number: M012
VanaCof 2CHLOPHEDIANOL HCL, DEXCHLORPHENIRAMINE MALEATEGM Pharmaceuticals, INC0c7c6756-abb2-c10c-e063-6394a90a98632026-01-08WarningsExact identifier
application number: M012
VANACOF XP Cough / Chest CongestionDEXTROMETHORPHAN HBR, GUAIFENESINGM Pharmaceuticals, INC0b3a8cc1-a49f-e1e5-e063-6394a90a1c062026-01-08WarningsExact identifier
application number: M012
Diphenhydramine HClDIPHENHYDRAMINE HCLINVAHEALTH INCe4e4004f-77e3-569d-e053-2a95a90a73fe2026-01-08WarningsExact identifier
application number: M012
Robitussin Maximum Strength Cough Plus Chest Congestion DMDEXTROMETHORPHAN HYDROBROMIDE AND GUAIFENESINHaleon US Holdings LLC868ac65a-63e2-46ac-b87d-66b2890867562026-01-08WarningsExact identifier
application number: M012
Theraflu Flu Relief Max Strength DaytimeACETAMINOPHEN, DEXTROMETHORPHAN HBRHaleon US Holdings LLC0324195f-506d-4747-990e-ad44e2a117d92026-01-07WarningsExact identifier
application number: M012
Sambrosa NightDOXYLAMINE SUCCINATESambrosa Care, Inc.acdc8740-6231-d1e8-e053-2995a90a3b8d2026-01-07WarningsExact identifier
application number: M012
VAPOREXCAMPHOR (SYNTHETIC), EUCALYPTUS OIL, AND MENTHOLDLC Laboratories, Inc.971943b1-4199-4f75-9d2d-61242d346b5f2026-01-07WarningsExact identifier
application number: M012
BACTIMICINA COUGH AND COLDDEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, AND PHENYLEPHRINE HYDROCHLORIDEDLC Laboratories, Inc.2e612c62-9bbb-45f2-a253-aa2bfaeaac702026-01-07WarningsExact identifier
application number: M012
Earths Care Chest RubCAMPHOR, EUCALYPTUS OI, MENTHOLDLC Laboratories, Inc2424f5d5-1772-96f1-e063-6294a90a89ee2026-01-07WarningsExact identifier
application number: M012
Bactimicina Vapor RubVAPOR RUBDLC Laboratories, Inc.176b617a-faf6-7893-e063-6294a90a046b2026-01-07WarningsExact identifier
application number: M012
Sinus Pressure and PainACETAMINOPHEN, PHENYLEPHRINE HCLFamily Dollar Services Inc0d3e4ceb-5059-4aac-8aa2-bf714ca9deb22026-01-07WarningsExact identifier
application number: M012
Tussin Multi Symptom Cold CFDEXTROMETHORPHAN HBR GUAIFENESIN PHENYLEPHRINE HCLQUALITY CHOICE (Chain Drug Marketing Association)b225e897-5728-4519-b727-c0f361c759762026-01-07WarningsExact identifier
application number: M012
Severe Cold and FluACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATE, PHENYLEPHRINE HCLWalgreen Company80b218f7-66bb-4e15-a0dc-ec9b6af1b0562026-01-07WarningsExact identifier
application number: M012
tussin cough and chest congestionDEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESINRite Aid Corporation13618054-d0c5-4190-b626-e7e91b8557382026-01-06WarningsExact identifier
application number: M012
Berkley and Jensen Tussin DM MaxDEXTROMETHORPHAN HBR, GUAIFENESINBJWCc15b97a8-968f-4d38-905e-863e9fd16ce62026-01-06WarningsExact identifier
application number: M012

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1049160pseudoephedrine HCl 30 MG Oral TabletPSN09feb5f0-c22d-4a1b-97a0-d5767e5f773010
1049162SudoGest 30 MG Oral TabletPSN09feb5f0-c22d-4a1b-97a0-d5767e5f773010
1049162pseudoephedrine hydrochloride 30 MG Oral Tablet [Sudogest]SBD09feb5f0-c22d-4a1b-97a0-d5767e5f773010
1049160pseudoephedrine hydrochloride 30 MG Oral TabletSCD09feb5f0-c22d-4a1b-97a0-d5767e5f773010
1049162Sudogest 30 MG Oral TabletSY09feb5f0-c22d-4a1b-97a0-d5767e5f773010

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
50090-4345-05009043450048 TABLET, FILM COATED in 1 BOTTLE (50090-4345-0) 2019-10-090000-00-00NoNoCurrent
50090-4345-15009043450124 BLISTER PACK in 1 CARTON (50090-4345-1) / 1 TABLET, FILM COATED in 1 BLISTER PACK24 blister pack2019-06-100000-00-00NoNoCurrent
50090-4345-25009043450212 TABLET, FILM COATED in 1 BOTTLE (50090-4345-2) 2019-10-090000-00-00NoNoCurrent
50090-4345-35009043450330 TABLET, FILM COATED in 1 BOTTLE (50090-4345-3) 2019-10-090000-00-00NoNoCurrent
50090-4345-4500904345044 TABLET, FILM COATED in 1 BOTTLE (50090-4345-4) 2019-10-090000-00-00NoNoCurrent
50090-4345-55009043450515 TABLET, FILM COATED in 1 BOTTLE (50090-4345-5) 2019-10-090000-00-00NoNoCurrent