FDA.reportPublic FDA data

NDC 61841-055 - 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
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 table
LabelManufacturerEffective dateType
THERAFLEX Glucosamine Plus Max Hard Gelatine CapsulesBayer HealthCare LLC.2026-01-12HUMAN OTC DRUG LABEL

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 Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
61841-055THERAFLEX GLUCOSAMINE PLUS MAX (D-GLUCOSAMINE HYDROCHLORIDE, CHONDROITIN SULFATE SODIUM1) CAPSULE [BAYER HEALTHCARE LLC.]106 package rows20240111_19d09bb6-f1e9-0477-e054-00144ff8d46c.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
CHONDROITIN SULFATE SODIUM (BOVINE)ACTIVE INGREDIENT8QTV3DTT8WTHERAFLEX GLUCOSAMINE PLUS MAX (D-GLUCOSAMINE HYDROCHLORIDE, CHONDROITIN SULFATE SODIUM1) CAPSULE [BAYER HEALTHCARE LLC, CONSUMER CARE]1
CHONDROITIN SULFATE (BOVINE)ACTIVE MOIETY6IC1M3OG5ZTHERAFLEX GLUCOSAMINE PLUS MAX (D-GLUCOSAMINE HYDROCHLORIDE, CHONDROITIN SULFATE SODIUM1) CAPSULE [BAYER HEALTHCARE LLC, CONSUMER CARE]1
MANGANESE SULFATEINACTIVE INGREDIENTW00LYS4T26THERAFLEX 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.

Matched openFDA labels page 2 of 2 · 35 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Vitrexyl plus IronFERROUS FUMARATE, FOLIC ACIDPureTek Corporationada43056-a3ce-e7de-e053-2a95a90aa0462023-01-11Warnings, Adverse reactionsExact identifier
unii: W00LYS4T26
PureVit DualFe PlusFERROUS FUMARATE, POLYSACCHARIDE IRON COMPLEXPureTek Corporation71f63741-cad4-43b5-bb3e-c63a188d10a22023-01-11Warnings, Adverse reactionsExact identifier
unii: W00LYS4T26
VitrexylFOLIC ACIDPureTek Corporationae064a9e-daba-fa86-e053-2a95a90a16a72023-01-11Warnings, Adverse reactionsExact identifier
unii: W00LYS4T26
Vitranol FeFERROUS FUMARATE, FOLIC ACIDPureTek Corporationb81daf17-430b-6ba2-e053-2a95a90a768b2023-01-11Warnings, Adverse reactionsExact identifier
unii: W00LYS4T26
VitrexateFOLIC ACIDPureTek Corporationb34fee43-bea9-45b7-e053-2a95a90aad4d2023-01-11Warnings, Adverse reactionsExact identifier
unii: W00LYS4T26
Vitrexate FEFERROUS FUMARATE, FOLIC ACIDPureTek Corporationb3637def-a701-673a-e053-2995a90a02d52023-01-11Warnings, Adverse reactionsExact identifier
unii: W00LYS4T26
VenexaFOLIC ACIDPureTek Corporationba130779-cdfd-086d-e053-2a95a90a25902023-01-11Warnings, Adverse reactionsExact identifier
unii: W00LYS4T26
Venexa FEFERROUS FUMARATE, FOLIC ACIDPureTek Corporationba142128-21c4-4204-e053-2a95a90ae0d72023-01-11Warnings, Adverse reactionsExact identifier
unii: W00LYS4T26
Ribotin-EFERROUS FUMARATE, FOLIC ACIDPureTek Corporationbb1492c5-bfcd-d632-e053-2a95a90ad7d12023-01-11Warnings, Adverse reactionsExact identifier
unii: W00LYS4T26
Ventrixyl FeFERROUS FUMARATE, FOLIC ACIDPureTek Corporationc7a626ec-88ec-d899-e053-2a95a90ab0ba2023-01-11Warnings, Adverse reactionsExact identifier
unii: W00LYS4T26
Zintrexyl-CFERROUS FUMARATE, FOLIC ACIDPureTek Corporationbb1492c5-bfca-d632-e053-2a95a90ad7d12023-01-11Warnings, Adverse reactionsExact identifier
unii: W00LYS4T26
Concept OBVITAMIN MINERAL SUPPLEMENTU.S. Pharmaceutical Corporation37992a25-68bd-4050-b936-596ddedc25a32022-11-08Warnings, Adverse reactionsExact identifier
unii: W00LYS4T26
Manganum SulphuricumMANGANUM SULPHURICUMHahnemann Laboratories, INC.e939792e-f82a-2cc1-e053-2995a90aac882022-09-21Exact identifier
unii: W00LYS4T26
Multitrace -4 PediatricTRACE ELEMENTS 4American Regent, Inc.5ee6a685-3c35-467b-8d4d-79efdd0bfa8e2019-04-25Warnings, Adverse reactionsExact identifier
unii: W00LYS4T26
Multitrace-5TRACE ELEMENTS 5American Regent, Inc.ef63bbe8-ebf8-436c-b38d-6cb92bc91ac02019-04-25Warnings, Adverse reactionsExact identifier
unii: W00LYS4T26

Reported adverse events (FAERS/openFDA)#

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