Statement of Identity section
SUPER JOINT FORTE
Glucosamine, Chondroitin, MSM, Hyaluronic Acid, Calcium Fructoborate Tablets
Innovative Joints Supporting Formula
Super Joint Forte
- Manufacturer
- Novel Pack LLC
- Effective date
- 2022-05-05
- Label type
- Dietary Supplement
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-06-01 02:50:27
Label at a glance#
ProductSuper Joint Forte
Active ingredientGLUCOSAMINE HYDROCHLORIDE, DIMETHYL SULFONE, CALCIUM FRUCTOBORATE, CHONDROITIN 6-SULFATE, HYALURONIC ACID
Label structure5 sections
Label contents#
Full prescribing information#
Dosage
Take 3 tablet daily with a meal or as directed by your healthcare professional.
"Not to exceed the recommended daily usuage."
Storage Declaration
Store in a cool, dry & dark place. Protect from direct sunlight and heat.
WARNINGS SECTION
Not to be used by children below 5 years of age.
Store out of rech of children
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 82489-106-01 | Super Joint Forte | 120 in 1 BOTTLE | TABLET | 120 | 1 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- Super Joint Forte
- Glucosamine, Chondroitin, MSM, Hyaluronic Acid, Calcium Fructoborate
- GLUCOSAMINE HYDROCHLORIDE
- GLUCOSAMINE
- DIMETHYL SULFONE
- CALCIUM FRUCTOBORATE
- CHONDROITIN 6-SULFATE
- HYALURONIC ACID
- MICROCRYSTALLINE CELLULOSE
- POLACRILIN POTASSIUM
- POVIDONE K30
- STARCH, CORN
- SODIUM STARCH GLYCOLATE TYPE A
- MAGNESIUM STEARATE
- TALC
- SILICON DIOXIDE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 82489-106 | 82489-106-01 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| GLUCOSAMINE HYDROCHLORIDE | 750W5330FY | ACTIB |
| DIMETHYL SULFONE | 9H4PO4Z4FT | ACTIB |
| CALCIUM FRUCTOBORATE | 7EW2EZ38LS | ACTIB |
| CHONDROITIN 6-SULFATE | 7LWQ6472SP | ACTIB |
| HYALURONIC ACID | S270N0TRQY | ACTIB |
| MICROCRYSTALLINE CELLULOSE | OP1R32D61U | IACT |
| POLACRILIN POTASSIUM | 0BZ5A00FQU | IACT |
| POVIDONE K30 | U725QWY32X | IACT |
| STARCH, CORN | O8232NY3SJ | IACT |
| SODIUM STARCH GLYCOLATE TYPE A | H8AV0SQX4D | IACT |
| MAGNESIUM STEARATE | 70097M6I30 | IACT |
| TALC | 7SEV7J4R1U | IACT |
| SILICON DIOXIDE | ETJ7Z6XBU4 | IACT |
Source Document#
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.