FDA.reportPublic FDA data

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 44 of 188 · 3,753 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Creosote Combination 9254CREOSOTE COMBINATIONProfessional Complementary Health Formulas9248c4d5-75a5-4b52-b6b1-b2b8af8da8272026-01-08WarningsExact identifier
unii: ETJ7Z6XBU4
Bridged Ring Combination 9311BRIDGED RING COMBINATIONProfessional Complementary Health Formulasb4033f70-d974-493d-8ded-eaa3240bdac52026-01-08WarningsExact identifier
unii: ETJ7Z6XBU4
Cell Salt Combination 8013CELL SALT COMBINATIONProfessional Complementary Health Formulasb3a33345-3c3d-4f86-ae4d-757c65fd1ed32026-01-08WarningsExact identifier
unii: ETJ7Z6XBU4
RET Heart 7009RET HEARTProfessional Complementary Health Formulase2bf8331-1c50-4216-93a4-1d3cf64047592026-01-08WarningsExact identifier
unii: ETJ7Z6XBU4
Lumbar Drops 5013LUMBAR DROPSProfessional Complementary Health Formulasee6b54ea-fb6a-4723-8a0f-970aa82fea802026-01-08WarningsExact identifier
unii: ETJ7Z6XBU4
unii: 1FW7WLR731
Rehydration Drops 2175REHYDRATION DROPSProfessional Complementary Health Formulas58cc2bd1-c530-43bf-876e-f30d4d95b8da2026-01-08WarningsExact identifier
unii: ETJ7Z6XBU4
Dysfunctional Bleeding Drops 2138DYSFUNCTIONAL BLEEDING DROPSProfessional Complementary Health Formulas3e674c1e-c64b-416d-962f-c03493e800852026-01-08WarningsExact identifier
unii: ETJ7Z6XBU4
A-L-O Liquid Drops 2082A-L-O LIQUID DROPSProfessional Complementary Health Formulas65e081be-4fc6-416b-aacd-55b194b77b3b2026-01-08WarningsExact identifier
unii: 1FW7WLR731
Cervical Drops 5002CERVICAL DROPSProfessional Complementary Health Formulasedd5f196-1423-4d4c-a8c1-89427c4f387e2026-01-08WarningsExact identifier
unii: ETJ7Z6XBU4
unii: 1FW7WLR731
Asbestox 6005ASBESTOXProfessional Complementary Health Formulas90bc0d00-01e4-4134-809e-e216fd09852a2026-01-08WarningsExact identifier
unii: ETJ7Z6XBU4
Ledum Combination 9257LEDUM COMBINATIONProfessional Complementary Health Formulas38b89b32-4915-487d-8b2d-250123487b152026-01-08WarningsExact identifier
unii: ETJ7Z6XBU4
Fourth Chakra (Heart) 7304FOURTH CHAKRA (HEART)Professional Complementary Health Formulasef061447-42ae-43d0-b6f3-bf19a96ffe922026-01-08WarningsExact identifier
unii: ETJ7Z6XBU4
Spinal Drops 5025SPINAL DROPSProfessional Complementary Health Formulasca6d7250-9c9e-40a6-8d41-88aba33d21dd2026-01-08WarningsExact identifier
unii: ETJ7Z6XBU4
Anti-Scar Drops 2084ANTI-SCAR DROPSProfessional Complementary Health Formulasad0e9159-ed68-48aa-a7d1-7ff5c32ec3042026-01-08WarningsExact identifier
unii: ETJ7Z6XBU4
Muscle/Ligament/Cartilage Drops 5015MUSCLE/LIGAMENT/CARTILAGE DROPSProfessional Complementary Health Formulasb82df0d2-9fee-4542-a0f7-c082912302542026-01-08WarningsExact identifier
unii: 6IC1M3OG5Z
unii: 1FW7WLR731
Fifth Chakra (Throat) 7305FIFTH CHAKRA (THROAT)Professional Complementary Health Formulasb731f708-10a8-451f-8550-1e7302102b962026-01-08WarningsExact identifier
unii: ETJ7Z6XBU4
Pain Formula Drops 2046PAIN FORMULA DROPSProfessional Complementary Health Formulas4456c022-5aac-49b4-b976-b629525f3d492026-01-08WarningsExact identifier
unii: WK2XYI10QM
Sixth Chakra (Third Eye) 7306SIXTH CHAKRA (THIRD EYE)Professional Complementary Health Formulas174024e7-e231-456c-bc00-48a358d7160a2026-01-08WarningsExact identifier
unii: ETJ7Z6XBU4
Injury Drops 2034INJURY DROPSProfessional Complementary Health Formulas024011a0-6471-4016-86d4-19eeb21f0d822026-01-08WarningsExact identifier
unii: ETJ7Z6XBU4
Third Chakra (Solar Plexus) 7303THIRD CHAKRA (SOLAR PLEXUS)Professional Complementary Health Formulaseea89c37-ab87-4cc7-8dfc-e7f42a580dd92026-01-08WarningsExact identifier
unii: ETJ7Z6XBU4

Reported adverse events (FAERS/openFDA)#

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