MedPath

JBA Joint Revive

Approved
Approval ID

27f5acf3-04f6-49d7-bbf5-f1c3ad6200cc

Product Type

HUMAN OTC DRUG LABEL

Effective Date

Mar 31, 2025

Manufacturers
FDA

Advanced Pharmaceutical Services, Inc. Dba Affordable Quality Pharmaceuticals

DUNS: 187498279

Products 1

Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.

Glucosamine Sulfate Potassium Chloride,White Willow Bark Extract,Eggshell Membrane Collagen,Chondroitin Sulfate,Turmeric Root Extract,Bromelain,Soy Lecithin

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code13411-856
Product Classification
G
Generic Name
Glucosamine Sulfate Potassium Chloride,White Willow Bark Extract,Eggshell Membrane Collagen,Chondroitin Sulfate,Turmeric Root Extract,Bromelain,Soy Lecithin
Product Specifications
Route of AdministrationORAL
Effective DateMarch 31, 2025
FDA Product Classification

INGREDIENTS (10)

STARCH, CORNInactive
Code: O8232NY3SJ
Classification: IACT
MICROCRYSTALLINE CELLULOSEInactive
Code: OP1R32D61U
Classification: IACT
SALIX ALBA BARKActive
Quantity: 160 mg in 1 1
Code: 205MXS71H7
Classification: ACTIB
EGG SHELL MEMBRANEActive
Quantity: 150 mg in 1 1
Code: N7QBR4212V
Classification: ACTIB
CHONDROITIN SULFATE (BOVINE)Active
Quantity: 100 mg in 1 1
Code: 6IC1M3OG5Z
Classification: ACTIB
TURMERICActive
Quantity: 50 mg in 1 1
Code: 856YO1Z64F
Classification: ACTIB
STEM BROMELAINActive
Quantity: 10 mg in 1 1
Code: ZLM4P8929R
Classification: ACTIB
MAGNESIUM STEARATEInactive
Code: 70097M6I30
Classification: IACT
GLUCOSAMINE SULFATE POTASSIUM CHLORIDEActive
Quantity: 300 mg in 1 1
Code: 15VQ11I66N
Classification: ACTIM
SOYBEAN LECITHINActive
Quantity: 5 mg in 1 1
Code: 1DI56QDM62
Classification: ACTIB

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JBA Joint Revive - FDA Drug Approval Details