FDA.reportPublic FDA data

THERAFLEX Glucosamine Plus Max Hard Gelatine Capsules

Manufacturer
Bayer HealthCare LLC.
Effective date
2026-01-12
Label type
HUMAN OTC DRUG LABEL
Version
11
Source
full-release
Hydrated at
2026-06-01 01:32:17

Label at a glance#

ProductTHERAFLEX Glucosamine Plus Max
Active ingredientCHONDROITIN SULFATE SODIUM (BOVINE)
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

theraflextheraflex

Foreign labelForeign label

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
0306390c-dd77-4363-afe0-63c58088b2a1Product name120220120
503ea967-4b9c-48cf-9e87-c7975295849dProduct name220220120

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
61841-055-12THERAFLEX Glucosamine Plus Max1 in 1 CARTONCAPSULE111
61841-055-12THERAFLEX Glucosamine Plus Max120 in 1 BOTTLECAPSULE12011
61841-055-30THERAFLEX Glucosamine Plus Max1 in 1 CARTONCAPSULE111
61841-055-30THERAFLEX Glucosamine Plus Max30 in 1 BOTTLECAPSULE3011
61841-055-60THERAFLEX Glucosamine Plus Max1 in 1 CARTONCAPSULE111
61841-055-60THERAFLEX Glucosamine Plus Max60 in 1 BOTTLECAPSULE6011

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
CHONDROITIN SULFATE SODIUM (BOVINE)ACTIVE INGREDIENT8QTV3DTT8W1
CHONDROITIN SULFATE (BOVINE)ACTIVE MOIETY6IC1M3OG5Z1
MANGANESE SULFATEINACTIVE INGREDIENTW00LYS4T261

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
61841-05561841-055-12, 61841-055-60, 61841-055-30

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
MANGANESE SULFATEW00LYS4T26IACT
CHONDROITIN SULFATE SODIUM (BOVINE)8QTV3DTT8WACTIM

Source Document#

Source XML

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.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
4833265b-4b7d-8e86-e063-6294a90a674019d09bb6-f1e9-0477-e054-00144ff8d46c2026-01-12Exact identifier
spl id: 4833265b-4b7d-8e86-e063-6294a90a6740
spl set id: 19d09bb6-f1e9-0477-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.