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 143 of 186 · 3,701 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
IBUPROFEN	IBUPROFEN	NuCare Pharmaceuticals,Inc.	99d7cf65-3ec2-24eb-e053-2a95a90acc5e	2024-06-20		Exact identifier unii: WK2XYI10QM
Ibuprofen	IBUPROFEN	NuCare Pharmaceuticals,Inc.	a2160213-2a32-2044-e053-2995a90a21af	2024-06-20	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: WK2XYI10QM
IBUPROFEN	IBUPROFEN 200MG	Lil' Drug Store Products, Inc.	8fc65767-1783-4f7f-8680-9e43ba4d5481	2024-06-19	Warnings	Exact identifier unii: WK2XYI10QM
Ibuprofen	IBUPROFEN	NuCare Pharmaceuticals,Inc.	8c3dccbb-1084-cd09-e053-2a95a90ac12a	2024-06-18	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: WK2XYI10QM
Ibuprofen	IBUPROFEN	NuCare Pharmaceuticals,Inc.	8cb93e5f-4ebc-24b7-e053-2a95a90a5a23	2024-06-18	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: WK2XYI10QM
Protectif Fair Tint	ZINC OXIDE AND TITANIUM DIOXIDE	Derma Research Group Inc.	1a8c8804-1d6b-b5a5-e063-6394a90a1260	2024-06-18	Warnings	Exact identifier unii: 15FIX9V2JP
Ibuprofen	IBUPROFEN	NuCare Pharmaceuticals,Inc.	88795f0e-41b7-504e-e053-2995a90a3b9e	2024-06-14	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: WK2XYI10QM
Protectif Untinted	ZINC OXIDE AND TITANIUM DIOXIDE	Derma Research Group Inc.	1acd3f09-87f2-75e4-e063-6394a90a0cd9	2024-06-13	Warnings	Exact identifier unii: 15FIX9V2JP
Cold Sore Rescue	BORAX, DULCAMARA, NATRUM MURIATICUM, RANUNCULUS BULBOSUS, SILICEA	Peaceful Mountain, Inc.	a7fe6ec7-a758-43cf-b46f-c327e0632fb8	2024-06-13	Warnings	Exact identifier unii: ETJ7Z6XBU4
Ibuprofen, Circle K, 50ct	IBUPROFEN	Lil' Drug Store Products, Inc.	1ab6fbae-ead5-283b-e063-6394a90a4ed4	2024-06-12	Warnings	Exact identifier unii: WK2XYI10QM
Ibuprofen	IBUPROFEN	Trifecta Pharmaceuticals USA LLC	114b5e23-6cd7-41d8-e063-6294a90aa0f0	2024-06-12	Warnings	Exact identifier unii: WK2XYI10QM
IBUPROFEN	IBUPROFEN	NuCare Pharmaceuticals,Inc.	6d86ce94-a06a-2769-e053-2991aa0afb95	2024-06-10		Exact identifier unii: WK2XYI10QM
SILICEA	SILICEA	Rxhomeo Private Limited d.b.a. Rxhomeo, Inc	1a361030-a925-0998-e063-6394a90a915d	2024-06-06	Warnings	Exact identifier unii: ETJ7Z6XBU4
Youth 3 Activating BB Cream SPF 30 Medium	ZINC OXIDE, TITANIUM DIOXIDE	Shaklee Corporation	ccc80ea4-f270-4fd4-970c-eaa63df936e4	2024-06-06	Warnings	Exact identifier unii: 15FIX9V2JP
IBUPROFEN	IBUPROFEN	NuCare Pharmaceuticals,Inc.	6365b2d6-2337-70c0-e053-2a91aa0aa960	2024-06-06		Exact identifier unii: WK2XYI10QM
toty Solaria Body	OCTINOXATE, OCTOCRYLENE, TITANIUM DIOXIDE, ZINC OXIDE	CHIPICAN LLC	1a121b17-3621-6bc1-e063-6394a90ac9a1	2024-06-04	Warnings	Exact identifier unii: 15FIX9V2JP
PROCEUTICALS PRIVATE LABEL by TiZO tinted mineral sunscreen	TITANIUM DIOXIDE, ZINC OXIDE	Fallien Cosmeceuticals, LTD	0b62062d-b77e-4e6c-b3ab-b35ab24db7cb	2024-06-04	Warnings	Exact identifier unii: 15FIX9V2JP
Ibuprofen	IBUPROFEN	Boswell Pharmacy Services LLC d/b/a BPS Wholesale	1a02fa34-b5ae-7183-e063-6294a90a3ae4	2024-06-03	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: WK2XYI10QM
ibuprofen	IBUPROFEN	SKYA HEALTH, LLC	1c28af16-7246-4e4c-a1be-939655c37242	2024-05-31	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: WK2XYI10QM
Protectif Deep Tint	ZINC OXIDE AND TITANIUM DIOXIDE	Derma Research Group Inc.	19b19023-1340-6609-e063-6394a90a6eaf	2024-05-30	Warnings	Exact identifier unii: 15FIX9V2JP

Reported adverse events (FAERS/openFDA)#

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