Nasal Decongestant
- Product NDC
- 50844-112
- 11-digit product format
- 508440112
- Labeler code
- 50844
- Product ID
- 50844-112_962e4e53-1137-48a6-888c-05bb0b5e648b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Pseudoephedrine HCl
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- L.N.K. International, Inc.
- Application
- M012
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 1981-08-25
- 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
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
- Nasal Decongestant
- Listing expiration
- 2026-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| PSEUDOEPHEDRINE HYDROCHLORIDE | 30 mg/1 |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| 6V9V2RYJ8N | Internal UNII lookup |
Harmonized RxCUI identifiers#
| Identifier | FDA.report destination |
|---|---|
| 1049160 | Internal RxNorm lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| f12b7f07-0b81-4cab-ae0f-43a7bf9b4bc5 | Available on FDA.report |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| ba088a92-ab5e-b2d4-e908-f5ea691b7587 | Product name | 7 | 20210201 |
| 0fdb98e2-b951-a1ce-5715-2b187ba500ef | Product name | 4 | 20170718 |
| e974e22d-8688-7d92-1e87-40c1079e170c | Product name | 3 | 20151125 |
| e8718272-64cb-4436-969b-176c3067c8f4 | Product name | 1 | 20150609 |
| 30c51294-7ae9-8007-7de6-58222684a0be | Product name | 1 | 20140508 |
| 4f26f669-fc6c-40ef-9e26-1c7b2390ee66 | Product name | 1 | 20140508 |
| 70a83adc-6047-bbea-5a08-dfd304aa47d2 | Product name | 1 | 20140508 |
| 858ce051-9941-aafc-8c7c-44a8e0227463 | Product name | 1 | 20140508 |
| b893258d-0942-3d8a-3411-056ea0788ff5 | Product name | 1 | 20140508 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 50844-112-08 | Nasal Decongestant | 12 in 1 BLISTER PACK | TABLET, FILM COATED | 12 | 19 | |
| 50844-112-08 | Nasal Decongestant | 2 in 1 CARTON | TABLET, FILM COATED | 2 | 19 | |
| 50844-112-22 | Nasal Decongestant | 12 in 1 BLISTER PACK | TABLET, FILM COATED | 12 | 19 | |
| 50844-112-22 | Nasal Decongestant | 4 in 1 CARTON | TABLET, FILM COATED | 4 | 19 | |
| 50844-112-46 | Nasal Decongestant | 8 in 1 CARTON | TABLET, FILM COATED | 8 | 19 | |
| 50844-112-46 | Nasal Decongestant | 12 in 1 BLISTER PACK | TABLET, FILM COATED | 12 | 19 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 50844-112-22 | EA - Each | 50844-112 | 3310c6ff-4340-4e26-8aa0-c254b60bed98 | 1 | 2022-06-06 |
| 50844-112-46 | EA - Each | 50844-112 | 9d0541ce-08ce-4cb0-8680-608ec5e8ee89 | 1 | 2022-06-06 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Theraflu Severe Congestion Relief Cooling Nasal Mist | OXYMETAZOLINE HCL | Haleon US Holdings LLC | 90125a19-eed7-4ca4-a6dc-f38026c74d54 | 2026-06-08 | Warnings | M012 |
| Severe Cold and Flu | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL | Walgreen Company | 54254b61-7861-4eeb-bd3c-54fd5266f4a7 | 2026-06-08 | Warnings | M012 |
| Guaifenesin | GUAIFENESIN | Major Pharmaceuticals | aa662428-e61f-4e22-af4d-8cf63df68c99 | 2026-06-08 | Warnings | M012 |
| Daytime Nighttime | ACETAMINOPHEN, GUAIFENESIN AND ACETAMINOPHEN, DEXTROMETHORPHAN HBR, TRIPROLIDINE HCL | TARGET CORPORATION | 47a218a0-6395-36bd-e063-6394a90a265a | 2026-06-05 | Warnings | M012 |
| Daytime Nighttime | ACETAMINOPHEN DEXTROMETHORPHAN HBR, ACETAMINOPHEN DEXTROMETHORPHAN HBR TRIPROLIDINE HCL | TARGET CORPORATION | 4779288a-9850-8490-e063-6394a90abe51 | 2026-06-05 | Warnings | M012 |
| Mucinex Fast-Max DM Max and Mucinex Fast-Max Nighttime DM Max Value Pack | DEXTROMETHORPHAN HBR, GUAIFENESIN AND TRIPROLIDINE HCL | Reckitt Benckiser LLC | 4df37cfb-299f-661f-e063-6394a90ab337 | 2026-06-04 | Warnings | M012 |
| ALKA SELTZER COLD Cold Flu Congestion Severe Fast Hot Liquid Day Night | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE, AND DOXYLAMINE SUCCINATE | Bayer HealthCare LLC. | 53715ea4-42b3-5887-e063-6294a90a4249 | 2026-06-04 | Warnings | M012 |
| Tussin DM | DEXTROMETHORPHAN HBR, GUAIFENESIN | Chain Drug Marketing Association, Inc. | b0d38db9-22a9-4dd8-8e0f-dd81805e724b | 2026-06-04 | Warnings | M012 |
| Cough and Cold HBP | CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HBR | CVS PHARMACY | 65d4d7ea-c080-404e-9836-7d6bdcc5ea7d | 2026-06-04 | Warnings | M012 |
| Allergy Relief Childrens | DIPHENHYDRAMINE HCL | CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED | fe9d6a6e-38a1-44ae-a30f-596c5ec7d057 | 2026-06-03 | Warnings | M012 |
| Severe Congestion and Cough | DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL | Walgreen Company | b0c1d635-0f85-433a-b479-51c68d259faa | 2026-06-03 | Warnings | M012 |
| Cold and Flu Nighttime | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, TRIPROLIDINE HCL | Walgreen Company | de4e8af4-d3d0-44b3-aea3-79016803ccdc | 2026-06-03 | Warnings | M012 |
| Mucus Relief DM | DEXTROMETHORPHAN HBR AND GUAIFENESIN | ARMY AND AIR FORCE EXCHANGE SERVICE | dc0a3761-bbe2-4261-a183-594f5fb12b0b | 2026-06-03 | Warnings | M012 |
| Cold and Flu Daytime, Nighttime | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, TRIPROLIDINE HCL | WALMART INC. | f278cc81-65b2-4e45-be5b-41152cbb67c4 | 2026-06-03 | Warnings | M012 |
| Allergy Relief | DIPHENHYDRAMINE HCL | Family Dollar Services Inc | 358ba91d-06a4-49c9-994d-4e4bf9499dcd | 2026-06-03 | Warnings | M012 |
| GUAIFENESIN DM | GUAIFENESIN AND DEXTROMETHORPHAN | Cardinal Health 107, LLC | c5fd53c9-81d6-4ce6-88a0-c2c24e17a7ed | 2026-06-02 | Warnings | M012 |
| ALKA SELTZER COLD Cold and Flu plus Congestion Severe Fast Hot Liquid Night | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE, AND PHENYLEPHRINE HYDROCHLORIDE | Bayer HealthCare LLC. | 5349dbde-730c-610f-e063-6394a90a952a | 2026-06-02 | Warnings | M012 |
| Guaifenesin and Codeine Phosphate | GUAIFENESIN AND CODEINE PHOSPHATE | Cardinal Health 107, LLC | a9130f36-4761-4e6b-a383-eca3db06ea93 | 2026-06-02 | Warnings | M012 |
| Topcare Day Time Nite Time Cold and Flu | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATE, GUAIFENESIN, PHENYLEPHRINE HCL | Topco Associates LLC | aed387e0-5a8b-4caf-a373-3e04496a4983 | 2026-06-02 | Warnings | M012 |
| ALKA SELTZER COLD Cold Flu And Congestion Severe Fast Hot Liquid Day | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, AND PHENYLEPHRINE HYDROCHLORIDE | Bayer HealthCare LLC. | 53371691-2510-5039-e063-6394a90a6ea9 | 2026-06-01 | Warnings | M012 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 1049160 | pseudoephedrine HCl 30 MG Oral Tablet | PSN | f12b7f07-0b81-4cab-ae0f-43a7bf9b4bc5 | 19 |
| 1049160 | pseudoephedrine hydrochloride 30 MG Oral Tablet | SCD | f12b7f07-0b81-4cab-ae0f-43a7bf9b4bc5 | 19 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 50844-112-08 | 50844011208 | 2 BLISTER PACK in 1 CARTON (50844-112-08) / 12 TABLET, FILM COATED in 1 BLISTER PACK | 2 blister pack | 1981-08-25 | 0000-00-00 | No | No | Current |
| 50844-112-22 | 50844011222 | 4 BLISTER PACK in 1 CARTON (50844-112-22) / 12 TABLET, FILM COATED in 1 BLISTER PACK | 4 blister pack | 1981-08-25 | 0000-00-00 | No | No | Current |
| 50844-112-46 | 50844011246 | 8 BLISTER PACK in 1 CARTON (50844-112-46) / 12 TABLET, FILM COATED in 1 BLISTER PACK | 8 blister pack | 1981-08-25 | 0000-00-00 | No | No | Current |