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 138 of 188 · 3,753 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Positive Light Tinted Moisturizer Broad Spectrum SPF 20 Sunscreen 44NHOMOSALATE, TITANIUM DIOXIDE, ZINC OXIDERare Beauty, LLCcffbb6af-5a04-f58a-e053-2995a90a1ae22024-10-23WarningsExact identifier
unii: 15FIX9V2JP
Banana BoatTITANIUM DIOXIDE, ZINC OXIDEEdgewell Personal Care Brands, LLC441a46f0-ecda-4448-e054-00144ff88e882024-10-23WarningsExact identifier
unii: 15FIX9V2JP
Positive Light Tinted Moisturizer Broad Spectrum SPF 20 Sunscreen 28CHOMOSALATE, TITANIUM DIOXIDE, ZINC OXIDERare Beauty, LLCcffb8219-7076-de64-e053-2a95a90a60362024-10-23WarningsExact identifier
unii: 15FIX9V2JP
Positive Light Tinted Moisturizer Broad Spectrum SPF 20 Sunscreen 10NHOMOSALATE, TITANIUM DIOXIDE, ZINC OXIDERare Beauty, LLCcfee02eb-92f9-be12-e053-2a95a90a43372024-10-23WarningsExact identifier
unii: 15FIX9V2JP
CVS Health 60 Plus Sensitive Skin SunTITANIUM DIOXIDE, ZINC OXIDECVS Pharmacy477c25ec-33db-04a6-e054-00144ff8d46c2024-10-22WarningsExact identifier
unii: 15FIX9V2JP
Bali Body Tinted Super Serum Natural SPF 30OCTISALATE, OCTOCRYLENE, TITANIUM DIOXIDE, ZINC OXIDEBali Body Pty Ltdf5eeaf37-33f2-2c0c-e053-2a95a90abcc02024-10-21WarningsExact identifier
unii: 15FIX9V2JP
IbuprofenIBUPROFENA-S Medication Solutions2d0c2d35-c212-4daa-b2c4-b407ca0b16ad2024-10-21Boxed warning, Warnings, Adverse reactionsExact identifier
unii: WK2XYI10QM
IbuprofenIBUPROFENA-S Medication Solutions2b470e48-c23c-4f5c-916a-d38d8518896b2024-10-21Boxed warning, Warnings, Adverse reactionsExact identifier
unii: WK2XYI10QM
Fruit of the Earth Sun Town City Baby and Kids Mineral SPF 50 SunscreenTITANIUM DIOXIDE, ZINC OXIDEFruit Of The Earth, Inc.f42a0b1e-038d-4fab-e053-2995a90a53642024-10-18WarningsExact identifier
unii: 15FIX9V2JP
Fruit of the Earth Sun Town City Mineral SPF 30 SunscreenTITANIUM DIOXIDE, ZINC OXIDEFruit Of The Earth, Inc.f4481bf3-6dc7-5641-e053-2a95a90ad9382024-10-18WarningsExact identifier
unii: 15FIX9V2JP
Fruit of the Earth Sun Town City Mineral SPF 50 SunscreenTITANIUM DIOXIDE, ZINC OXIDEFruit Of The Earth, Inc.f45d25d2-9305-5858-e053-2a95a90a7f7b2024-10-18WarningsExact identifier
unii: 15FIX9V2JP
SPF50 Plus Mineral SunscreenZINC OXIDE AND TITANIUM DIOXIDEKAS Direct LLC dba BabyGanics08e8bc10-85d8-4215-8351-7ec12029416c2024-10-17WarningsExact identifier
unii: 15FIX9V2JP
MINERAL SUNSCREEN SPF 50ZINC OXIDE, TITANIUM DIOXIDEWEGMANS FOOD MARKETS INCbfe24f55-d0e5-254a-e053-2995a90a2fd32024-10-16WarningsExact identifier
unii: 15FIX9V2JP
Equate Sunscreen SPF 50 KIDS Broad SpectrumTITANIUM DIOXIDE, ZINC OXIDEWAL-MART STORES INC81cb6b2e-1ca3-4a83-a8df-9bfee61e79af2024-10-16WarningsExact identifier
unii: 15FIX9V2JP
MINERAL BASED SPF 50 SUNSCREENZINC OXIDE, TITANIUM DIOXIDETHE KROGER COMPANYa4e6936d-a76c-e8fd-e053-2995a90a965f2024-10-15WarningsExact identifier
unii: 15FIX9V2JP
TopCare Everyday Mineral Sunscreen Continuous Broad Spectrum SPF 50 Reef-Conscious FormulaTITANIUM DIOXIDE, ZINC OXIDETOPCO ASSOCIATES LLCf14f43e6-ee57-5495-e053-2a95a90a40112024-10-15WarningsExact identifier
unii: 15FIX9V2JP
MINERAL SUNSCREEN SPF 50ZINC OXIDE, TITANIUM DIOXIDETOPCO ASSOCIATES LLCbfe076fa-f21f-2c46-e053-2a95a90acee42024-10-15WarningsExact identifier
unii: 15FIX9V2JP
H.E.B. Mineral Sunscreen Broad Spectrum SPF 50TITANIUM DIOXIDE, ZINC OXIDEH.E.B.c5279caf-3af9-d163-e053-2995a90a943b2024-10-15WarningsExact identifier
unii: 15FIX9V2JP
kirkland signature ibuprofen ibIBUPROFENCostco Wholesale Company2fee0f32-0bc7-4d98-b5d4-5a7dad1c2a2c2024-10-14WarningsExact identifier
unii: WK2XYI10QM
Target Up and Up Mineral Sunscreen Broad Spectrum SPF 50 Reef-Conscious FormulaTITANIUM DIOXIDE, ZINC OXIDETARGET CORPORATIONcfd735d2-df3a-5ed0-e053-2995a90a9f262024-10-14WarningsExact identifier
unii: 15FIX9V2JP

Reported adverse events (FAERS/openFDA)#

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