TRIPROLIDINE HYDROCHLORIDE
- Product NDC
- 69367-253
- 11-digit product format
- 693670253
- Labeler code
- 69367
- Product ID
- 69367-253_2ef4d962-1c92-48e3-bf24-200a275b3d08
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- TRIPROLIDINE HYDROCHLORIDE
- Dosage form
- SYRUP
- Route
- ORAL
- Labeler
- Westminster Pharmaceuticals, LLC
- Application
- M012
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2020-03-09
- Substance
- TRIPROLIDINE HYDROCHLORIDE
- Active strength
- .938 mg/mL
- 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
- TRIPROLIDINE HYDROCHLORIDE
- Listing expiration
- 2027-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| TRIPROLIDINE HYDROCHLORIDE | .938 mg/mL |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| YAN7R5L890 | Internal UNII lookup |
Harmonized RxCUI identifiers#
| Identifier | FDA.report destination |
|---|---|
| 1491649 | Internal RxNorm lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| a9f01760-e335-4410-a9b8-8edce2841270 | Available on FDA.report |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| 30c51294-7ae9-8007-7de6-58222684a0be | Product name | 1 | 20140508 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 69367-253-30 | TRIPROLIDINE HYDROCHLORIDE | 30 mL in 1 BOTTLE, DROPPER | SYRUP | 30 | 6 | |
| 69367-253-30 | TRIPROLIDINE HYDROCHLORIDE | 1 in 1 CARTON | SYRUP | 1 | 6 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 69367-253-30 | ML - Milliliter | 69367-253 | 62c5665b-aceb-4eef-8490-9ce397066f0d | 1 | 2020-06-05 |
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 |
|---|---|---|---|---|---|---|
| Cherry Cough Drop | MENTHOL | Safeway Inc. | 4a52c0c2-8659-2819-e054-00144ff8d46c | 2025-12-20 | Warnings | M012 |
| Signature Care Cherry Cough Drops | MENTHOL | Safeway | a733e905-af15-d3ea-e053-2a95a90aa7c3 | 2025-12-20 | Warnings | M012 |
| Signature Care Honey Lemon Cough Drops | MENTHOL | Safeway | a742449f-c76b-2b91-e053-2a95a90ae4d2 | 2025-12-20 | Warnings | M012 |
| Cherry Sore Throat Lozenge | BENZOCAINE | TopCo | 60b876e7-c642-5ce8-e053-2a91aa0abd6e | 2025-12-20 | Warnings | M012 |
| menthol cough drops | MENTHOL | Topco Associates | 366cc6b1-beff-29d2-e054-00144ff88e88 | 2025-12-20 | Warnings | M012 |
| cherry cough drops | MENTHOL | TopCo Associates | 3fef2117-7311-1e66-e054-00144ff8d46c | 2025-12-20 | Warnings | M012 |
| honey lemon cough drops | MENTHOL | Topco Associates | 3ff1bf05-e407-3b67-e054-00144ff8d46c | 2025-12-20 | Warnings | M012 |
| sugar free menthol cough drops | MENTHOL | Topco Associates | 36727f0c-d6d2-28a3-e054-00144ff8d46c | 2025-12-20 | Warnings | M012 |
| sugar free honey lemon cough drops | MENTHOL | Topco Associates | 36824bee-607e-7095-e054-00144ff8d46c | 2025-12-20 | Warnings | M012 |
| Mixed Berry Sore Throat Lozenges | BENZOCAINE | Topco Associates | 7a00c771-9231-e877-e053-2a91aa0ac96e | 2025-12-20 | Warnings | M012 |
| MUCUS RELIEF | GUAIFENESIN 400 MG | NUVICARE LLC | e25b440e-f389-443f-b333-c66ad1747158 | 2025-12-19 | Warnings | M012 |
| Cold and Flu severe | ACETAMINOPHEN,DEXTROMETHORPHAN HBR,GUAIFENESIN,PHENYLEPHRINE HCL | Wal-Mart Stores Inc | 9fca25dc-f63e-487a-8b7c-84d65ea51cb5 | 2025-12-19 | Warnings | M012 |
| Cold and Flu Severe | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL | Geiss, Destin & Dunn Inc. | a7d2eaee-484e-43aa-8ae3-0e050219383f | 2025-12-19 | Warnings | M012 |
| Cherry Cough Drops | MENTHOL | Publix | 66d8e5f7-9766-57f3-e053-2991aa0a7e17 | 2025-12-19 | Warnings | M012 |
| Honey Lemon Cough Drops | MENTHOL | Publix | 66e89fa3-ee09-1d16-e053-2a91aa0ae17c | 2025-12-19 | Warnings | M012 |
| Poly-Vent DM | DEXTROMETHORPHAN HBR, GUAIFENESIN AND PSEUDOEPHEDRINE HCL | Poly Pharmaceuticals, Inc. | 739329ae-0b62-4eab-a07d-867b5d3d61e0 | 2025-12-19 | Warnings | M012 |
| Chest Congestion and Cough Relief DM | DEXTROMETHORPHAN HBR, GUAIFENESIN | ARMY AND AIR FORCE EXCHANGE SERVICE | 89494a7c-cdbf-48f1-aaa9-2e57d4388a68 | 2025-12-19 | Warnings | M012 |
| DayTime Cold/Flu Relief | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCL | ARMY AND AIR FORCE EXCHANGE SERVICE | 04f9134e-1311-4843-90db-9244b9e61e1d | 2025-12-19 | Warnings | M012 |
| Nighttime Cold/Flu Relief | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATE | ARMY AND AIR FORCE EXCHANGE SERVICE | 029e6215-b72d-4fd0-8918-db1abcc4490a | 2025-12-19 | Warnings | M012 |
| DayTime and Nighttime Cold/Flu Relief Softgels - Combo Pack | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCL, DOXYLAMINE SUCCINATE | ARMY AND AIR FORCE EXCHANGE SERVICE | 5f680f37-b3db-450f-b8ca-f9e31a04dc04 | 2025-12-19 | Warnings | M012 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 1491649 | triprolidine HCl 0.938 MG in 1 mL Oral Solution | PSN | a9f01760-e335-4410-a9b8-8edce2841270 | 6 |
| 1491649 | triprolidine hydrochloride 0.938 MG/ML Oral Solution | SCD | a9f01760-e335-4410-a9b8-8edce2841270 | 6 |
Packages#
| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 69367-253-30 | 69367025330 | 1 BOTTLE, DROPPER in 1 CARTON (69367-253-30) / 30 mL in 1 BOTTLE, DROPPER | 2020-03-09 | 0000-00-00 | No | No | Current |