NDC 76162-680 - MAXIMUM STRENGTH Sinus Relief Day and Night SOFTGELS - 24 ct
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
- 76162-680
- Manufacturer
- Topco Associates LLC
- Effective date
- 2025-12-10
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Sinus Relief Day - Topco Associates LLC | Topco Associates LLC | 2025-12-10 | HUMAN OTC DRUG LABEL |
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 |
|---|---|---|---|---|---|---|
| No Drip Severe Anefrin Nasal | 0.05% OXYMETAZOLINE HCL | Walgreens Company | c126e969-56f3-47b4-a011-02ff150eccb8 | 2024-08-02 | Warnings | M012 |
| Mucus Relief DM | GUAIFENESIN, DEXTROMETHORPHAN HBR | H E B | 20df2ffe-5281-4cd6-adb3-3a3d28788ef6 | 2024-08-02 | Warnings | 9D2RTI9KYH 495W7451VQ |
| Mucus Relief DM | GUAIFENESIN, DEXTROMETHORPHAN HBR | H E B | bcc41783-9213-4a8e-b7db-75b4da08551d | 2024-08-02 | Warnings | 9D2RTI9KYH 495W7451VQ |
| Mucus Relief DM | GUAIFENESIN, DEXTROMETHORPHAN HBR | H E B | 187097bf-37c8-4184-a2fd-1eff9147d370 | 2024-08-01 | Warnings | 9D2RTI9KYH 495W7451VQ |
| Essential Sheer SPF 50 | ZINC OXIDE TITANIUM DIOXIDE | Topiderm, Inc. | 2132dc18-85ee-4449-86d2-d9f698f286c6 | 2024-07-31 | Warnings | 15FIX9V2JP |
| Acetaminophen Extra Strength | ACETAMINOPHEN | FSA STORE INC. | 1cd6a3e6-1376-0b7b-e063-6394a90af3d1 | 2024-07-30 | Warnings | 362O9ITL9D |
| Proceuticals Private Label by TiZO tinted foaming mineral sunscreen | TITANIUM DIOXIDE, ZINC OXIDE | Fallien Cosmeceuticals, Ltd | 1e78109f-4d2e-2705-e063-6294a90a5ad3 | 2024-07-30 | Warnings | 15FIX9V2JP |
| Replenix Sheer SPF 50 | ZINC OXIDE TITANIUM DIOXIDE | Topiderm, Inc. | 37d1f454-3bc9-4ce5-863c-0d4f6fa18fb4 | 2024-07-29 | Warnings | 15FIX9V2JP |
| nasal | OXYMETAZOLINE HYDROCHLORIDE | Rite Aid Corporation | 90e0426b-654f-4bcd-8b1d-cf56d1fc0c68 | 2024-07-27 | Warnings | M012 |
| Guaifenesin 600 mg | GUAIFENESIN | Dr. Reddy's Laboratories Inc. | 99307c61-5df3-0a83-1e21-ddb03bc905b4 | 2024-07-26 | Warnings | 495W7451VQ |
| Mucinex | GUAIFENESIN | American Health Packaging | 0129f47d-abc2-414c-b4e1-1064c5d6a623 | 2024-07-25 | Warnings | 495W7451VQ |
| 8 Hour Pain Relief | ACETAMINOPHEN | AMERISOURCE BERGEN | 9ab903aa-7170-460b-9527-e3df223f5f55 | 2024-07-24 | Warnings | 362O9ITL9D |
| ACETAMINOPHEN AND CODEINE PHOSPHATE | ACETAMINOPHEN AND CODEINE PHOSPHATE | NuCare Pharmaceuticals, Inc. | 1e01f923-38c1-9b59-e063-6394a90a22f1 | 2024-07-24 | Boxed warning, Warnings, Adverse reactions | 362O9ITL9D |
| nasal decongestant | OXYMETAZOLINE HCL | A-S Medication Solutions | 0e81a937-59e5-4869-8ffb-c758fb37230d | 2024-07-23 | Warnings | M012 |
| ACETAMINOPHEN | ACETAMINOPHEN | GERI-CARE PHARMACEUTICAL CORP | 92c22593-daf9-20a8-e053-2a95a90a365d | 2024-07-23 | Warnings | 362O9ITL9D |
| WesTussin DM | DEXCHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCL | Westminster Pharmaceuticals, LLC | 68a0cd44-3fdd-430e-af1a-498d4415ab78 | 2024-07-23 | Warnings | M012 9D2RTI9KYH 04JA59TNSJ |
| Allergy Relief | DIPHENHYDRAMINE HCL 25 MG | Lil' Drug Store Products, Inc. | edc244d6-eb0b-d3c9-e053-2a95a90a2622 | 2024-07-22 | Warnings | M012 |
| Night Time Sleep Aid | DIPHENHYDRAMINE HCL | Dolgencorp, Inc. (DOLLAR GENERAL & REXALL) | 1f3eeb6c-4c44-4e2a-ad72-12c95e6589c9 | 2024-07-22 | Warnings | M012 |
| CareOne Childrens Allergy Relief | DIPHENHYDRAMINE HCL | American Sales Company | bb78ef2c-4f42-4e8f-b38d-f9b2965a384b | 2024-07-19 | Warnings | M012 |
| dg health allergy childrens | DIPHENHYDRAMINE HYDROCHLORIDE | Dolgencorp, LLC | 71445443-34bd-4d8c-b9c8-e7c3b8d4c832 | 2024-07-19 | Warnings | M012 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.