Home NDC 13411-858 JBA Joint Revive TM The Legend Caffe Latte
Product NDC 13411-858
11-digit product format 134110858
Labeler code 13411
Product ID 13411-858_44a86e5f-f79b-d5aa-e063-6294a90af830
Type HUMAN OTC DRUG
Nonproprietary name Glucosamine Sulfate Potassium Chloride,Chondroitin Sulfate,Fucoidan Extract
Dosage form POWDER
Route ORAL
Labeler Advanced Pharmaceutical Services, Inc. Dba Affordable Quality Pharmaceuticals
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2024-10-28
Substance CHONDROITIN SULFATE (BOVINE); GLUCOSAMINE SULFATE POTASSIUM CHLORIDE; LAMINARIA JAPONICA
Active strength 1000; 1500; 500 mg/1; mg/1; mg/1
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base JBA Joint Revive TM The Legend Caffe Latte
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength LAMINARIA JAPONICA 1000 mg/1 CHONDROITIN SULFATE (BOVINE) 1500 mg/1 GLUCOSAMINE SULFATE POTASSIUM CHLORIDE 500 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination WE98HW412B Internal UNII lookup 6IC1M3OG5Z Internal UNII lookup 15VQ11I66N Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 13411-858-15 JBA Joint Revive TM The Legend Caffe Latte 15 in 1 BOX POWDER 15 2 13411-858-30 JBA Joint Revive TM The Legend Caffe Latte 30 in 1 BOX POWDER 30 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 13411-858 JBA JOINT REVIVE TM THE LEGEND CAFFE LATTE (GLUCOSAMINE SULFATE POTASSIUM CHLORIDE,CHONDROITIN SULFATE,FUCOIDAN EXTRACT) POWDER [ADVANCED PHARMACEUTICAL SERVICES, INC. DBA AFFORDABLE QUALITY PHARMACEUTICALS] 1 Current NDC, 2 package rows 20241101_fd397678-084e-4cde-8785-d96325634cdd.zip
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.
Matched openFDA labels page 1 of 1 · 1 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 13411-858-15 13411085815 15 POWDER in 1 BOX (13411-858-15) 15 powder 2024-10-28 No No Current 13411-858-30 13411085830 30 POWDER in 1 BOX (13411-858-30) 30 powder 2024-10-28 No No Current