NDC 81033-003-40 - Diphenhydramine Hydrochloride
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 81033-003
- Requested NDC
- 81033-003-40
- Package NDCs from labels
- 81033-003-05, 81033-003-50, 81033-003-52, 81033-003-10, 81033-003-40, 81033-003-41
- Manufacturer
- Kesin Pharma Corporation
- Effective date
- 2023-01-16
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Diphenhydramine Hydrochloride - Kesin Pharma Corporation | Kesin Pharma Corporation | 2023-01-16 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 81033-003-41 | 2024-07-30 | C162847 | 48780-1 | 1e7a6dab-189d-a2ce-e063-dadaa90aadf7 | Diphenhydramine HCl 2.5mg/mL Unit Dose Cups, 12.5mg/5 mL, 25mg/10mL |
| 81033-003-52 | 2024-07-30 | C162847 | 48780-1 | 1e7a6dab-189d-a2ce-e063-dadaa90aadf7 | Diphenhydramine HCl 2.5mg/mL Unit Dose Cups, 12.5mg/5 mL, 25mg/10mL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 81033-003-05 | Diphenhydramine Hydrochloride | 5 mL in 1 CUP, UNIT-DOSE | LIQUID | 5 | 2 | |
| 81033-003-10 | Diphenhydramine Hydrochloride | 10 mL in 1 CUP, UNIT-DOSE | LIQUID | 10 | 2 | |
| 81033-003-40 | Diphenhydramine Hydrochloride | 40 in 1 CARTON | LIQUID | 40 | 2 | |
| 81033-003-41 | Diphenhydramine Hydrochloride | 8 in 1 CASE | LIQUID | 8 | 2 | |
| 81033-003-50 | Diphenhydramine Hydrochloride | 50 in 1 CARTON | LIQUID | 50 | 2 | |
| 81033-003-52 | Diphenhydramine Hydrochloride | 8 in 1 CASE | LIQUID | 8 | 2 |
DailyMed Dashboard NDC Coverage#
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 81033-003-05 | ML - Milliliter | 81033-003 | f3701be5-9a5c-438f-b934-93806d66ebd4 | 1 | 2021-10-08 |
| 81033-003-10 | ML - Milliliter | 81033-003 | 5d902f8f-3bc7-4bea-914d-2933d9172d09 | 1 | 2021-10-08 |
| 81033-003-40 | ML - Milliliter | 81033-003 | 7ba3f437-e501-4726-9cbd-0f7dde860113 | 1 | 2021-10-08 |
| 81033-003-50 | ML - Milliliter | 81033-003 | 29f4b183-8acf-4b5d-9c82-ef7967038684 | 1 | 2021-10-08 |
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 |
|---|---|---|---|---|---|---|
| Soothe Chewable | CITRIC ACID | Carolina Cannabis Creations LLC | 04a78060-7f0d-c4bd-e063-6294a90ae152 | 2025-01-15 | Warnings | 2968PHW8QP |
| Soothe Chewable | CITRIC ACID | Carolina Cannabis Creations LLC | 04a78a5c-e3b5-f362-e063-6394a90a0807 | 2025-01-15 | Warnings | 2968PHW8QP |
| D-99 | ATROPA BELLADONNA, NITROGLYCERIN, LACTIC ACID, UNSPECIFIED FORM, SCROPHULARIA NODOSA, ALOE, RADIUM BROMIDE, POTASSIUM IODIDE, SUS SCROFA BONE MARROW, ZINC, AND CITRIC ACID MONOHYDRATE | DNA Labs, Inc. | dd9c0226-35ea-445a-a570-1ec35551f68d | 2025-01-13 | Warnings | 2968PHW8QP |
| D-97 | ALUMINUM OXIDE, SILVER, SILVER NITRATE, ARSENIC TRIOXIDE, MERCURIUS SOLUBILIS, CALOMEL, MERCURIC IODIDE, LEAD, LEAD IODIDE, CHELIDONIUM MAJUS, ZINC, SOLIDAGO VIRGAUREA FLOWERING TOP, AND CITRIC ACID MONOHYDRATE | DNA Labs, Inc. | b2079abb-786c-4f92-8d49-5606c77f7d72 | 2025-01-13 | Warnings | 2968PHW8QP |
| Diphenhydramine HCL | DIPHENHYDRAMINE HCL | SDA Laboratories, Inc. | 437e6a13-a4ff-4f98-8973-042f224ee85e | 2025-01-13 | Warnings | TC2D6JAD40 |
| Diphenhydramine HCL | DIPHENHYDRAMINE HCL | SDA Laboratories, Inc. | 6a520986-1004-4ee6-9a47-1dfd90bb1b2c | 2025-01-13 | Warnings | TC2D6JAD40 |
| Allergy Relief 25 mg | DIPHENHYDRAMINE HCL 25MG | Ulai Health LLC | 751f13d4-c4d6-47a5-b40d-1563de08c048 | 2025-01-12 | Warnings | TC2D6JAD40 |
| Anti-Itch Cream | DIPHENHYDRAMINE HYDROCHLORIDE 2%, ZINC ACETATE 0.1% | Chain Drug Marketing Association Inc. | 2b48cb2f-e6bf-f9de-e063-6394a90a42d4 | 2025-01-09 | Warnings | TC2D6JAD40 |
| SleepAid (Diphenhydramine HCL) | DIPHENHYDRAMINE HCL | APNAR PHARMA LP | faaf5d51-d81d-3acc-e053-6294a90ae08f | 2025-01-09 | Warnings | TC2D6JAD40 |
| STERILE WATER | STERILE WATER | HF Acquisition Co. LLC, DBA HealthFirst | 74ed2a6f-824c-a1ff-e053-2a91aa0a57c0 | 2025-01-09 | Warnings, Adverse reactions | 059QF0KO0R |
| STERILE WATER | STERILE WATER | HF Acquisition Co LLC, DBA HealthFirst | 77bd3c0f-f4ab-7cfa-e053-2a91aa0a1b83 | 2025-01-09 | Warnings, Adverse reactions | 059QF0KO0R |
| STERILE WATER | STERILE WATER | HF Acquisition Co LLC, DBA HealthFirst | 7610bf80-61b7-982f-e053-2a91aa0ac1bb | 2025-01-09 | Warnings, Adverse reactions | 059QF0KO0R |
| ANTI-ITCH | ZINC ACETATE , DIPHENHYDRAMINE | OL PHARMA TECH, LLC | b79d3096-c609-e710-e053-2995a90a8da2 | 2025-01-09 | Warnings | TC2D6JAD40 |
| T-27 | WATER | DNA Labs, Inc. | f0e9afd7-64a4-4b85-9c5f-4bf07ba4b481 | 2025-01-09 | Warnings | 059QF0KO0R |
| Hemorrhoidal Cream with Aloe | GLYCEROL, PHENYLEPHINE, PRAMOXINE, PETROLATUM | Chain Drug Marketing Association | 2b33c710-ac17-20f9-e063-6294a90ad29c | 2025-01-08 | Warnings | PDC6A3C0OX |
| ANTIBACTERIAL DREAMY FLORALS | GLYCERIN | Quimicas Handal de Centroamerica SA de CV | 09f73bec-516d-90f0-e063-6394a90aecab | 2025-01-08 | Warnings | PDC6A3C0OX |
| Sterile Water | STERILE WATER FOR INJECTION | Medefil, Inc. | 99e99a50-82d5-aff6-e053-2a95a90a8c56 | 2025-01-08 | Warnings, Adverse reactions | 059QF0KO0R |
| BACTERIOSTATIC WATER | BACTERIOSTATIC WATER | HF Acquisition Co LLC, DBA HealthFirst | 99b0ef9b-600a-40dc-e053-2a95a90aa07e | 2025-01-08 | Warnings, Adverse reactions | 059QF0KO0R |
| STERILE WATER | STERILE WATER | HF Acquisition Co LLC, DBA HealthFirst | 99b1cb12-0b2d-0c0f-e053-2a95a90ac3b6 | 2025-01-08 | Warnings, Adverse reactions | 059QF0KO0R |
| Emetrol Powder Non-Drowsy | SODIUM CITRATE DIHYDRATE | WellSpring Pharmaceutical Corporation | 9d8d2ee7-9db7-4be7-8c73-511eb2e32459 | 2025-01-08 | Warnings | B22547B95K |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.