NDC 61841-055-60 - THERAFLEX Glucosamine Plus Max
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
- 61841-055
- Requested NDC
- 61841-055-60
- Package NDCs from labels
- 61841-055-12, 61841-055-60, 61841-055-30
- Manufacturer
- Bayer HealthCare LLC.
- Effective date
- 2026-01-12
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| THERAFLEX Glucosamine Plus Max Hard Gelatine Capsules | Bayer HealthCare LLC. | 2026-01-12 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 61841-055-12 | THERAFLEX Glucosamine Plus Max | 1 in 1 CARTON | CAPSULE | 1 | 11 | |
| 61841-055-12 | THERAFLEX Glucosamine Plus Max | 120 in 1 BOTTLE | CAPSULE | 120 | 11 | |
| 61841-055-30 | THERAFLEX Glucosamine Plus Max | 1 in 1 CARTON | CAPSULE | 1 | 11 | |
| 61841-055-30 | THERAFLEX Glucosamine Plus Max | 30 in 1 BOTTLE | CAPSULE | 30 | 11 | |
| 61841-055-60 | THERAFLEX Glucosamine Plus Max | 1 in 1 CARTON | CAPSULE | 1 | 11 | |
| 61841-055-60 | THERAFLEX Glucosamine Plus Max | 60 in 1 BOTTLE | CAPSULE | 60 | 11 |
DailyMed Dashboard NDC Coverage#
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| CHONDROITIN SULFATE SODIUM (BOVINE) | ACTIVE INGREDIENT | 8QTV3DTT8W | THERAFLEX GLUCOSAMINE PLUS MAX (D-GLUCOSAMINE HYDROCHLORIDE, CHONDROITIN SULFATE SODIUM1) CAPSULE [BAYER HEALTHCARE LLC, CONSUMER CARE] | 1 | |
| CHONDROITIN SULFATE (BOVINE) | ACTIVE MOIETY | 6IC1M3OG5Z | THERAFLEX GLUCOSAMINE PLUS MAX (D-GLUCOSAMINE HYDROCHLORIDE, CHONDROITIN SULFATE SODIUM1) CAPSULE [BAYER HEALTHCARE LLC, CONSUMER CARE] | 1 | |
| MANGANESE SULFATE | INACTIVE INGREDIENT | W00LYS4T26 | THERAFLEX GLUCOSAMINE PLUS MAX (D-GLUCOSAMINE HYDROCHLORIDE, CHONDROITIN SULFATE SODIUM1) CAPSULE [BAYER HEALTHCARE LLC, CONSUMER CARE] | 1 |
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 |
|---|---|---|---|---|---|---|
| PNV Prenatol | MULTIVITAMIN | PureTek Corporation | 583f0194-0306-f31b-e063-6394a90a2a10 | 2026-08-06 | Warnings, Adverse reactions | W00LYS4T26 |
| Vitramyn | FOLIC ACID | PureTek Corporation | c8af7616-5178-6df0-e053-2a95a90a334d | 2026-06-18 | Warnings, Adverse reactions | W00LYS4T26 |
| Vitalux | MULTIVITAMIN | PureTek Corporation | 52d5eee7-8146-cc62-e063-6394a90a8c3f | 2026-06-02 | Boxed warning, Adverse reactions | W00LYS4T26 |
| Multitam | FOLIC ACID | PureTek Corporation | cee15842-4a9e-c6ba-e053-2a95a90aebc5 | 2026-04-13 | Warnings, Adverse reactions | W00LYS4T26 |
| 4833265b-4b7d-8e86-e063-6294a90a6740 | 19d09bb6-f1e9-0477-e054-00144ff8d46c | 2026-01-12 | 4833265b-4b7d-8e86-e063-6294a90a6740 19d09bb6-f1e9-0477-e054-00144ff8d46c | |||
| BM Manganese sulfate (Mang Sulf) | MANGANESE SULFATE | BM Private Limited | 38043162-2a06-440e-e063-6394a90aa587 | 2025-12-02 | Warnings | W00LYS4T26 |
| Bestmade Natural Products Manganese Sulfate (Mang Sulf) | MANGANESE SULFATE | Bestmade Natural Products | 2fad0266-2102-9c98-e063-6394a90a51ab | 2025-05-26 | Warnings | W00LYS4T26 |
| Se-Tan PLUS | MULTIVITAMIN/MINERAL | Seton Pharmaceuticals | 56e912df-3a49-4405-8df1-7b80d12bd920 | 2025-04-24 | Boxed warning, Adverse reactions | W00LYS4T26 |
| Ventrixyl | FOLIC ACID | PureTek Corporation | c29dc729-93be-2a20-e053-2a95a90a8ca3 | 2024-12-03 | Warnings, Adverse reactions | W00LYS4T26 |
| Folitin-Z | FERROUS FUMARATE, FOLIC ACID | PureTek Corporation | bb141ac2-e5df-4df4-e053-2995a90a6e72 | 2024-12-02 | Warnings, Adverse reactions | W00LYS4T26 |
| Foliflex | FERROUS FUMARATE, FOLIC ACID | PureTek Corporation | cba98d1a-8cf9-39d9-e053-2995a90ae8bb | 2024-11-27 | Warnings, Adverse reactions | W00LYS4T26 |
| Finazol | FERROUS FUMARATE, FOLATE | PureTek Corporation | 24290823-022a-433b-e063-6394a90a8fd0 | 2024-11-07 | Warnings, Adverse reactions | W00LYS4T26 |
| Prenatryl | FERROUS FUMARATE, FOLIC ACID | PureTek Corporation | b364551b-2ccc-4db3-e053-2995a90afbbf | 2024-10-08 | Boxed warning, Adverse reactions | W00LYS4T26 |
| Prenatrix | FERROUS FUMARATE, FOLIC ACID | PureTek Corporation | ae07585b-e6e4-fd6d-e053-2995a90a7eec | 2024-09-30 | Boxed warning, Adverse reactions | W00LYS4T26 |
| Pretrate | FERROUS FUMARATE, FOLIC ACID | PureTek Corporation | ba4a1424-0782-77c0-e053-2a95a90a6e44 | 2024-09-30 | Boxed warning, Adverse reactions | W00LYS4T26 |
| Dexatran | MULTIVITAMIN | PureTek Corporation | e052d2c2-7a3f-37be-e053-2a95a90af21c | 2024-09-13 | Warnings, Adverse reactions | W00LYS4T26 |
| Multrys | TRACE ELEMENTS INJECTION 4 | American Regent, Inc. | 995f1efa-aca0-4b6c-9099-f8e757c2133a | 2024-07-01 | Warnings, Adverse reactions | W00LYS4T26 |
| Tralement | TRACE ELEMENTS INJECTION 4 | American Regent, Inc. | a49ffb90-f307-433e-a86e-aaea6d6a9982 | 2024-07-01 | Warnings, Adverse reactions | W00LYS4T26 |
| Prenatol-M | MULTIVITAMIN | PureTek Corporation | 17559a44-94b7-9ca0-e063-6294a90a2123 | 2024-05-06 | Warnings, Adverse reactions | W00LYS4T26 |
| Multitol-M | MULTIVITAMIN, FOLATE | PureTek Corporation | 163fdc9e-a405-c3ee-e063-6294a90afd49 | 2024-04-17 | Warnings, Adverse reactions | W00LYS4T26 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.