Nasal Decongestant
- Product NDC
- 50844-112
- 11-digit product format
- 508440112
- Labeler code
- 50844
- Product ID
- 50844-112_478a22dd-e80a-44c4-abb3-ec361d945afd
- 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
- 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
- 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 |
|---|---|---|---|---|---|---|
| Childrens Mucus Relief Cough Cherry Liquid | DEXTROMETHORPHAN HBR, GUAIFENSIN | Topco Associates | 3170748e-b09f-4c07-9927-df43771166c5 | 2025-12-16 | Warnings | M012 |
| Cold and Flu Nighttime | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE | QUALITY CHOICE (Chain Drug Marketing Association) | ca6d43cf-0d1f-4d3c-be7e-e3ac6a24f4fe | 2025-12-16 | Warnings | M012 |
| Cold and Flu Nighttime | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE | QUALITY CHOICE (Chain Drug Marketing Association) | e70d0784-53bc-4910-aade-3c9ad6e36441 | 2025-12-16 | Warnings | M012 |
| Pain and Sinus | ACETAMINOPHEN AND PHENYLEPHRINE | JHK Inc dba American Safety & First Aid | 88f86f5a-cc2b-4c75-b7a4-f2021922280b | 2025-12-16 | Warnings | M012 |
| Severe Congestion and Cough, Cold and Flu Nighttime | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL, TRIPROLIDINE HCL | Walgreen Company | b75af815-9bd4-4a7a-bc68-f42f4af50699 | 2025-12-16 | Warnings | M012 |
| Cough Relief Nighttime | DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE | QUALITY CHOICE (Chain Drug Marketing Association) | fe5fd29e-7f81-4633-8c3b-010d68abe701 | 2025-12-16 | Warnings | M012 |
| Mucus Relief Severe Congestion and Cough Maximum Strength | DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE | Harris Teeter, LLC | e0a62fa1-9f8a-4770-b28b-1f4f02a762e0 | 2025-12-16 | Warnings | M012 |
| Allergy Relief | DIPHENHYDRAMINE HCL | Walgreen Company | 8c4b59b8-dfab-4f4a-9966-f07b026a758a | 2025-12-16 | Warnings | M012 |
| Daytime Cold and Flu Non Drowsy | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE | QUALITY CHOICE (Chain Drug Marketing Association) | df866cf6-0526-4e61-ac9b-245b57dd5df6 | 2025-12-16 | Warnings | M012 |
| Severe Cold and Flu Relief Daytime | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE | Walgreens | c89200b6-4adb-452e-b931-07f631dad641 | 2025-12-16 | Warnings | M012 |
| ONESSIP ADULT DAYTIME SEVERE COLD AND FLU | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCI | MEDWISE LIFESCIENCES INC. | 45fa9159-d74c-063a-e063-6294a90a3ed0 | 2025-12-15 | Warnings | M012 |
| SudoGest Nasal Decongestant | PSEUDOEPHEDRINE HCL | Major Pharmaceuticals | 5229f4b2-a194-46f8-a0bc-4510fbe52075 | 2025-12-15 | Warnings | M012 |
| Topcare Nasal | OXYMETAZOLINE HYDROCHLORIDE | Topco Associates LLC | f2b2467f-2d9b-4742-b90a-95975c3b694f | 2025-12-13 | Warnings | M012 |
| Menthol Cough Drop | MENTHOL | HEB | 39178eb7-ada9-30bf-e054-00144ff88e88 | 2025-12-13 | Warnings | M012 |
| SF Menthol Cough Drop | MENTHOL | HEB | 3a443179-b7a6-3242-e054-00144ff8d46c | 2025-12-13 | Warnings | M012 |
| Cherry cough drop | MENTHOL | HEB | 39bd0ca1-348f-0ce1-e054-00144ff88e88 | 2025-12-13 | Warnings | M012 |
| Strawberry Cough Drops | MENTHOL | HEB | 766236e2-3302-2232-e053-2991aa0af503 | 2025-12-13 | Warnings | M012 |
| Honey Lemon Cough Drop | MENTHOL | HEB | 3a30a427-6ab4-24ae-e054-00144ff88e88 | 2025-12-13 | Warnings | M012 |
| Mixed Berry Sore Throat and Cough Lozenges | BENZOCAINE | HEB | 3063ea93-6bc2-1d18-e054-00144ff88e88 | 2025-12-13 | Warnings | M012 |
| HEB Menthol Cough Drops | MENTHOL | HEB | c197855d-15b4-38fc-e053-2a95a90a2dc7 | 2025-12-13 | 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 |