NDC 61841-152 - Theraflex Advance

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
61841-152
Package NDCs from labels
61841-152-72, 61841-152-12
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™ AdvanceBayer HealthCare LLC.2026-01-12HUMAN OTC DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
61841-152-12Theraflex Advance1 in 1 CARTONTABLET17
61841-152-12Theraflex Advance120 in 1 BOTTLETABLET1207
61841-152-72Theraflex Advance1 in 1 CARTONTABLET17
61841-152-72Theraflex Advance60 in 1 BOTTLETABLET607

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
61841-152THERAFLEX ADVANCE (IBUPROFEN, GLUCOSAMINE SULFATE, AND CHONDROITIN SULFATE (BOVINE)) TABLET [BAYER HEALTHCARE LLC.]64 package rows20240111_8fbde87b-d0d9-4a62-b8a3-9320cbb727a5.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
CHONDROITIN SULFATE (BOVINE)ACTIVE INGREDIENT6IC1M3OG5ZTHERAFLEX ADVANCE (IBUPROFEN, GLUCOSAMINE SULFATE, AND CHONDROITIN SULFATE (BOVINE)) TABLET [BAYER HEALTHCARE CONSUMER CARE]2
GLUCOSAMINE SULFATEACTIVE INGREDIENT1FW7WLR731THERAFLEX ADVANCE (IBUPROFEN, GLUCOSAMINE SULFATE, AND CHONDROITIN SULFATE (BOVINE)) TABLET [BAYER HEALTHCARE CONSUMER CARE]2
IBUPROFENACTIVE INGREDIENTWK2XYI10QMTHERAFLEX ADVANCE (IBUPROFEN, GLUCOSAMINE SULFATE, AND CHONDROITIN SULFATE (BOVINE)) TABLET [BAYER HEALTHCARE CONSUMER CARE]2
CONDOLIASEACTIVE MOIETY7SI2UZG934THERAFLEX ADVANCE (IBUPROFEN, GLUCOSAMINE SULFATE, AND CHONDROITIN SULFATE (BOVINE)) TABLET [BAYER HEALTHCARE CONSUMER CARE]2
GLUCOSAMINEACTIVE MOIETYN08U5BOQ1KTHERAFLEX ADVANCE (IBUPROFEN, GLUCOSAMINE SULFATE, AND CHONDROITIN SULFATE (BOVINE)) TABLET [BAYER HEALTHCARE CONSUMER CARE]2
IBUPROFENACTIVE MOIETYWK2XYI10QMTHERAFLEX ADVANCE (IBUPROFEN, GLUCOSAMINE SULFATE, AND CHONDROITIN SULFATE (BOVINE)) TABLET [BAYER HEALTHCARE CONSUMER CARE]2
CELLULOSE, MICROCRYSTALLINEINACTIVE INGREDIENTOP1R32D61UTHERAFLEX ADVANCE (IBUPROFEN, GLUCOSAMINE SULFATE, AND CHONDROITIN SULFATE (BOVINE)) TABLET [BAYER HEALTHCARE CONSUMER CARE]2
CROSPOVIDONEINACTIVE INGREDIENT68401960MKTHERAFLEX ADVANCE (IBUPROFEN, GLUCOSAMINE SULFATE, AND CHONDROITIN SULFATE (BOVINE)) TABLET [BAYER HEALTHCARE CONSUMER CARE]2
FD&C BLUE NO. 1INACTIVE INGREDIENTH3R47K3TBDTHERAFLEX ADVANCE (IBUPROFEN, GLUCOSAMINE SULFATE, AND CHONDROITIN SULFATE (BOVINE)) TABLET [BAYER HEALTHCARE CONSUMER CARE]2
GELATININACTIVE INGREDIENT2G86QN327LTHERAFLEX ADVANCE (IBUPROFEN, GLUCOSAMINE SULFATE, AND CHONDROITIN SULFATE (BOVINE)) TABLET [BAYER HEALTHCARE CONSUMER CARE]2
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I30THERAFLEX ADVANCE (IBUPROFEN, GLUCOSAMINE SULFATE, AND CHONDROITIN SULFATE (BOVINE)) TABLET [BAYER HEALTHCARE CONSUMER CARE]2
SILICON DIOXIDEINACTIVE INGREDIENTETJ7Z6XBU4THERAFLEX ADVANCE (IBUPROFEN, GLUCOSAMINE SULFATE, AND CHONDROITIN SULFATE (BOVINE)) TABLET [BAYER HEALTHCARE CONSUMER CARE]2
STARCH, CORNINACTIVE INGREDIENTO8232NY3SJTHERAFLEX ADVANCE (IBUPROFEN, GLUCOSAMINE SULFATE, AND CHONDROITIN SULFATE (BOVINE)) TABLET [BAYER HEALTHCARE CONSUMER CARE]2
STEARIC ACIDINACTIVE INGREDIENT4ELV7Z65APTHERAFLEX ADVANCE (IBUPROFEN, GLUCOSAMINE SULFATE, AND CHONDROITIN SULFATE (BOVINE)) TABLET [BAYER HEALTHCARE CONSUMER CARE]2
TITANIUM DIOXIDEINACTIVE INGREDIENT15FIX9V2JPTHERAFLEX ADVANCE (IBUPROFEN, GLUCOSAMINE SULFATE, AND CHONDROITIN SULFATE (BOVINE)) TABLET [BAYER HEALTHCARE CONSUMER CARE]2

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 99 of 188 · 3,753 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Dolce and Gabbana Everlast Foundation SPF 20 06W LightOCTISALATE, OCTOCRYLENE, TITANIUM DIOXIDE, ZINC OXIDEDolce & Gabbana Beauty S.R.L3090422e-fc18-45b8-88f2-6a9b282a72052025-08-04WarningsExact identifier
unii: 15FIX9V2JP
Dolce and Gabbana Everlast Foundation SPF 20 05N LightOCTISALATE, OCTOCRYLENE, TITANIUM DIOXIDE, ZINC OXIDEDolce & Gabbana Beauty S.R.Lf93aa5d2-90ab-4e11-874e-2ede4b25c4b62025-08-04WarningsExact identifier
unii: 15FIX9V2JP
Dolce and Gabbana Everlast Foundation SPF 20 04C LightOCTISALATE, OCTOCRYLENE, TITANIUM DIOXIDE, ZINC OXIDEDolce & Gabbana Beauty S.R.Lf055cd51-7b1d-43df-8990-8f60ba1eb91c2025-08-04WarningsExact identifier
unii: 15FIX9V2JP
Dolce and Gabbana Everlast Foundation SPF 20 07N LightOCTISALATE, OCTOCRYLENE, TITANIUM DIOXIDE, ZINC OXIDEDolce & Gabbana Beauty S.R.Ld4c76bc5-205b-45fd-8a02-4f4b174585032025-08-04WarningsExact identifier
unii: 15FIX9V2JP
CHILDRENS IBUPROFENIBUPROFENMeijer, Inc.eed4f13d-4bee-4ccc-a651-a6f86d6d1f7b2025-08-04WarningsExact identifier
unii: WK2XYI10QM
IbuprofenIBUPROFENAsclemed USA, Inc.d7ed42c4-371c-4a54-ab15-0630656f04272025-08-02Boxed warning, Warnings, Adverse reactionsExact identifier
unii: WK2XYI10QM
IbuprofenIBUPROFENPHOENIX RX LLC3b17587e-b609-42a9-e063-6294a90ab1f82025-08-01Boxed warning, Warnings, Adverse reactionsExact identifier
unii: WK2XYI10QM
Childrens Ibuprofen Oral SuspensionIBUPROFENPAI Holdings, LLC dba PAI Pharmac26cefe0-182a-4b03-baeb-b3eb2e0e22672025-08-01WarningsExact identifier
unii: WK2XYI10QM
Ibuprofen and famotidineIBUPROFEN AND FAMOTIDINEPreferred Pharmaceuticals Inc.e2f29ca9-9ec8-4b82-8c80-8628d9e3ab2f2025-08-01Boxed warning, Warnings, Adverse reactionsExact identifier
unii: WK2XYI10QM
Acetaminophen, IbuprofenACETAMINOPHEN, IBUPROFENGLENMARK THERAPEUTICS INC., USA57a8dc2b-a3bc-49fa-b605-2330155bdbff2025-07-31WarningsExact identifier
unii: WK2XYI10QM
IbuprofenIBUPROFENDolgencorp, Inc. (DOLLAR GENERAL & REXALL)0e95aab9-3a7c-49c3-b8df-f66d6f31aee02025-07-31WarningsExact identifier
unii: WK2XYI10QM
IbuprofenIBUPROFENRite Aid Corporation47657d95-4a54-49c2-8273-86b413b8f41e2025-07-30WarningsExact identifier
unii: WK2XYI10QM
Neutrogena Mineral Invisible Daily Defense Face Sunscreen Broad Spectrum SPF 30TITANIUM DIOXIDE, ZINC OXIDEKenvue Brands LLC003123d2-9675-fdd2-e063-6294a90a01302025-07-28WarningsExact identifier
unii: 15FIX9V2JP
Neutrogena Mineral Ultra Sheer Face SPF 70TITANIUM DIOXIDE, ZINC OXIDEKenvue Brands LLC20e0badf-fe25-1d27-e063-6294a90a7cfe2025-07-28WarningsExact identifier
unii: 15FIX9V2JP
Cell SaltsCALC. FLUOR., CALC. PHOS., CALC.SULPH., FERRUM PHOSPHORICUM, KALI MUR., KALI PHOS., KALI SULPH., MAG. PHOS., NAT. MUR., NAT. PHOS., NAT.SULPHURICUM, SILICEANewton Laboratories, Inc.985a3341-0fe0-1dd6-e053-2a95a90ad2c52025-07-25WarningsExact identifier
unii: ETJ7Z6XBU4
Dolce and Gabbana Everlast Foundation SPF 20 01N LightOCTISALATE, OCTOCRYLENE, TITANIUM DIOXIDE, ZINC OXIDEDolce & Gabbana Beauty S.R.L2ccf4e45-4cec-417d-9f4c-28f376025f1d2025-07-25WarningsExact identifier
unii: 15FIX9V2JP
SILICA MARINASILICON DIOXIDEBoiron3aada26e-6a8e-f545-e063-6394a90a9f802025-07-24Exact identifier
unii: ETJ7Z6XBU4
SunscreenTITANIUM DIOXIDE 6.8%Baxter of California, LLC146030bc-2bf4-25ea-e063-6294a90a46132025-07-24WarningsExact identifier
unii: 15FIX9V2JP
Cell SaltsCALC. FLUOR., CALC. PHOS., CALC.SULPH., FERRUM PHOSPHORICUM, KALI MUR., KALI PHOS., KALI SULPH., MAG. PHOS., NAT. MUR., NAT. PHOS., NAT.SULPHURICUM, SILICEANewton Laboratories, Inc.7a1b4e96-c96f-6424-e053-2991aa0aef302025-07-24WarningsExact identifier
unii: ETJ7Z6XBU4
Cell SaltsCALC. FLUOR., CALC. PHOS., CALC.SULPH., FERRUM PHOSPHORICUM, KALI MUR., KALI PHOS., KALI SULPH., MAG. PHOS., NAT. MUR., NAT. PHOS., NAT.SULPHURICUM, SILICEANewton Laboratories, Inc.7a1a9ef9-9a54-5f94-e053-2a91aa0ab4772025-07-24WarningsExact identifier
unii: ETJ7Z6XBU4

Reported adverse events (FAERS/openFDA)#

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