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
Label	Manufacturer	Effective date	Type
Theraflex™ Advance	Bayer HealthCare LLC.	2026-01-12	HUMAN OTC DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
61841-152-12	Theraflex Advance	1 in 1 CARTON	TABLET	1	7
61841-152-12	Theraflex Advance	120 in 1 BOTTLE	TABLET	120	7
61841-152-72	Theraflex Advance	1 in 1 CARTON	TABLET	1	7
61841-152-72	Theraflex Advance	60 in 1 BOTTLE	TABLET	60	7

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
61841-152	THERAFLEX ADVANCE (IBUPROFEN, GLUCOSAMINE SULFATE, AND CHONDROITIN SULFATE (BOVINE)) TABLET [BAYER HEALTHCARE LLC.]	6	4 package rows	20240111_8fbde87b-d0d9-4a62-b8a3-9320cbb727a5.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
CHONDROITIN SULFATE (BOVINE)	ACTIVE INGREDIENT	6IC1M3OG5Z	THERAFLEX ADVANCE (IBUPROFEN, GLUCOSAMINE SULFATE, AND CHONDROITIN SULFATE (BOVINE)) TABLET [BAYER HEALTHCARE CONSUMER CARE]	2
GLUCOSAMINE SULFATE	ACTIVE INGREDIENT	1FW7WLR731	THERAFLEX ADVANCE (IBUPROFEN, GLUCOSAMINE SULFATE, AND CHONDROITIN SULFATE (BOVINE)) TABLET [BAYER HEALTHCARE CONSUMER CARE]	2
IBUPROFEN	ACTIVE INGREDIENT	WK2XYI10QM	THERAFLEX ADVANCE (IBUPROFEN, GLUCOSAMINE SULFATE, AND CHONDROITIN SULFATE (BOVINE)) TABLET [BAYER HEALTHCARE CONSUMER CARE]	2
CONDOLIASE	ACTIVE MOIETY	7SI2UZG934	THERAFLEX ADVANCE (IBUPROFEN, GLUCOSAMINE SULFATE, AND CHONDROITIN SULFATE (BOVINE)) TABLET [BAYER HEALTHCARE CONSUMER CARE]	2
GLUCOSAMINE	ACTIVE MOIETY	N08U5BOQ1K	THERAFLEX ADVANCE (IBUPROFEN, GLUCOSAMINE SULFATE, AND CHONDROITIN SULFATE (BOVINE)) TABLET [BAYER HEALTHCARE CONSUMER CARE]	2
IBUPROFEN	ACTIVE MOIETY	WK2XYI10QM	THERAFLEX ADVANCE (IBUPROFEN, GLUCOSAMINE SULFATE, AND CHONDROITIN SULFATE (BOVINE)) TABLET [BAYER HEALTHCARE CONSUMER CARE]	2
CELLULOSE, MICROCRYSTALLINE	INACTIVE INGREDIENT	OP1R32D61U	THERAFLEX ADVANCE (IBUPROFEN, GLUCOSAMINE SULFATE, AND CHONDROITIN SULFATE (BOVINE)) TABLET [BAYER HEALTHCARE CONSUMER CARE]	2
CROSPOVIDONE	INACTIVE INGREDIENT	68401960MK	THERAFLEX ADVANCE (IBUPROFEN, GLUCOSAMINE SULFATE, AND CHONDROITIN SULFATE (BOVINE)) TABLET [BAYER HEALTHCARE CONSUMER CARE]	2
FD&C BLUE NO. 1	INACTIVE INGREDIENT	H3R47K3TBD	THERAFLEX ADVANCE (IBUPROFEN, GLUCOSAMINE SULFATE, AND CHONDROITIN SULFATE (BOVINE)) TABLET [BAYER HEALTHCARE CONSUMER CARE]	2
GELATIN	INACTIVE INGREDIENT	2G86QN327L	THERAFLEX ADVANCE (IBUPROFEN, GLUCOSAMINE SULFATE, AND CHONDROITIN SULFATE (BOVINE)) TABLET [BAYER HEALTHCARE CONSUMER CARE]	2
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	THERAFLEX ADVANCE (IBUPROFEN, GLUCOSAMINE SULFATE, AND CHONDROITIN SULFATE (BOVINE)) TABLET [BAYER HEALTHCARE CONSUMER CARE]	2
SILICON DIOXIDE	INACTIVE INGREDIENT	ETJ7Z6XBU4	THERAFLEX ADVANCE (IBUPROFEN, GLUCOSAMINE SULFATE, AND CHONDROITIN SULFATE (BOVINE)) TABLET [BAYER HEALTHCARE CONSUMER CARE]	2
STARCH, CORN	INACTIVE INGREDIENT	O8232NY3SJ	THERAFLEX ADVANCE (IBUPROFEN, GLUCOSAMINE SULFATE, AND CHONDROITIN SULFATE (BOVINE)) TABLET [BAYER HEALTHCARE CONSUMER CARE]	2
STEARIC ACID	INACTIVE INGREDIENT	4ELV7Z65AP	THERAFLEX ADVANCE (IBUPROFEN, GLUCOSAMINE SULFATE, AND CHONDROITIN SULFATE (BOVINE)) TABLET [BAYER HEALTHCARE CONSUMER CARE]	2
TITANIUM DIOXIDE	INACTIVE INGREDIENT	15FIX9V2JP	THERAFLEX 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 165 of 186 · 3,701 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
bareMinerals Original Foundation Broad Spectrum SPF 15 Fair Ivory	TITANIUM DIOXIDE	Orveon Global US LLC	15c92bce-75f4-40e3-ae28-9bcbc241c8e9	2023-10-04	Warnings	Exact identifier unii: 15FIX9V2JP
bareMinerals Complexion Rescue Defense Radiant Protective Veil Broad Spectrum SPF 30 Soft Radiance	TITANIUM DIOXIDE AND ZINC OXIDE	Orveon Global US LLC	0c2db44d-8604-4883-ab01-f14bc441e4e4	2023-10-04	Warnings	Exact identifier unii: 15FIX9V2JP
bareMinerals Original Foundation Broad Spectrum SPF 15 Medium Beige 12	TITANIUM DIOXIDE AND ZINC OXIDE	Orveon Global US LLC	3c35fd13-1a4b-4acf-ada4-16ee2e52dd94	2023-10-04	Warnings	Exact identifier unii: 15FIX9V2JP
bareMinerals Prime Time BB Primer-Cream Broad Spectrum SPF 30 Medium	TITANIUM DIOXIDE AND ZINC OXIDE	Orveon Global US LLC	3cc5b952-4619-4395-97c0-5b68efa9af6d	2023-10-04	Warnings	Exact identifier unii: 15FIX9V2JP
bareMinerals Skinlongevity Vital Power Moisturizer Broad Spectrum SPF 30	TITANIUM DIOXIDE AND ZINC OXIDE	Orveon Global US LLC	29c25bc3-902a-41af-996a-8c7e8a4bf574	2023-10-04	Warnings	Exact identifier unii: 15FIX9V2JP
bareMinerals Original Foundation Broad Spectrum SPF 15 Fairly Light 03	TITANIUM DIOXIDE	Orveon Global US LLC	b2909888-5a98-4894-a895-230aa53f64d9	2023-10-04	Warnings	Exact identifier unii: 15FIX9V2JP
bareMinerals Original Foundation Broad Spectrum SPF 15 Tan 19	TITANIUM DIOXIDE AND ZINC OXIDE	Orveon Global US LLC	a5888955-f381-4209-9589-bd2e79a84f59	2023-10-04	Warnings	Exact identifier unii: 15FIX9V2JP
bareMinerals Original Foundation Broad Spectrum SPF 15 Light 08	TITANIUM DIOXIDE AND ZINC OXIDE	Orveon Global US LLC	ad15bdee-67e6-4281-8144-e84b7c478a34	2023-10-04	Warnings	Exact identifier unii: 15FIX9V2JP
bareMinerals Original Foundation Broad Spectrum SPF 15 Medium Tan 18	TITANIUM DIOXIDE AND ZINC OXIDE	Orveon Global US LLC	aa4d7945-6cc9-4f20-b588-a5588e57d30a	2023-10-04	Warnings	Exact identifier unii: 15FIX9V2JP
bareMinerals Original Foundation Broad Spectrum SPF 15 Golden Tan 20	TITANIUM DIOXIDE AND ZINC OXIDE	Orveon Global US LLC	2f8b6c57-dcae-408e-898d-d5630deeb090	2023-10-04	Warnings	Exact identifier unii: 15FIX9V2JP
bareMinerals Original Foundation Broad Spectrum SPF 15 Golden Fair 04	TITANIUM DIOXIDE AND ZINC OXIDE	Orveon Global US LLC	e486915b-8097-451a-a018-3279213239b3	2023-10-04	Warnings	Exact identifier unii: 15FIX9V2JP
bareMinerals Original Foundation Broad Spectrum SPF 15 Golden Deep 28	TITANIUM DIOXIDE AND ZINC OXIDE	Orveon Global US LLC	5b51df09-40c3-4064-96d3-b7366fc83826	2023-10-04	Warnings	Exact identifier unii: 15FIX9V2JP
bareMinerals Original Foundation Broad Spectrum SPF 15 Fairly Medium 05	TITANIUM DIOXIDE AND ZINC OXIDE	Orveon Global US LLC	f1714e23-030c-4bd9-b9e7-111c3813ed34	2023-10-04	Warnings	Exact identifier unii: 15FIX9V2JP
bareMinerals Original Foundation Broad Spectrum SPF 15 Medium Dark 23	TITANIUM DIOXIDE AND ZINC OXIDE	Orveon Global US LLC	828fe263-f223-45c3-9710-fd8d59ad56b1	2023-10-04	Warnings	Exact identifier unii: 15FIX9V2JP
bareMinerals Multi-Tasking SPF 20 Concealer Bisque	TITANIUM DIOXIDE	Orveon Global US LLC	d4c30bea-8c56-4ed8-8ec4-f1b1e0e456dd	2023-10-04	Warnings	Exact identifier unii: 15FIX9V2JP
BareMinerals Mineral Veil	TITANIUM DIOXIDE AND ZINC OXIDE	Orveon Global US LLC	64b163dd-8a86-483f-8dab-80fa8740b12f	2023-10-04	Warnings	Exact identifier unii: 15FIX9V2JP
Ibuprofen and Diphenhydramine HCl	IBUPROFEN, DIPHENHYDRAMINE HCL	VALU MERCHANDISERS COMPANY	fed2f7ae-2827-f967-e053-6294a90adc0a	2023-10-03	Warnings	Exact identifier unii: WK2XYI10QM
Ibuprofen	IBUPROFEN	BETTER LIVING BRANDS, LLC	eb613c44-e125-0f40-e053-2995a90a7ca5	2023-10-02	Warnings	Exact identifier unii: WK2XYI10QM
Ibuprofen	IBUPROFEN	BETTER LIVING BRANDS, LLC	eb60e636-41fe-49fb-e053-2a95a90a0616	2023-09-29	Warnings	Exact identifier unii: WK2XYI10QM
BHI Migraine	ACETIC ACID, ARANEUS DIADEMATUS, ASAFETIDA, BRYONIA ALBA WHOLE, TRIBASIC CALCIUM PHOSPHATE, ACTIVATED CHARCOAL, CINCHONA OFFICINALIS BARK, MARSDENIA CONDURANGO BARK, TUBOCURARINE CHLORIDE, KALMIA LATIFOLIA LEAF, LYCOPODIUM CLAVATUM SPORE, SODIUM SULFATE, PHOSPHORIC ACID, PULSATILLA VULGARIS, CLAVICEPS PURPUREA SCLEROTIUM, AND SILICON DIOXIDE	MediNatura Inc	11cad8ba-6914-420e-bab0-4ca37d33f2e6	2023-09-28	Warnings	Exact identifier unii: ETJ7Z6XBU4

Reported adverse events (FAERS/openFDA)#

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