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 172 of 186 · 3,701 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Ibuprofen	IBUPROFEN	INGLES MARKETS, INC.	ef536841-768c-919f-e053-2a95a90af599	2022-12-12	Warnings	Exact identifier unii: WK2XYI10QM
Diphenhydramine HCl and Ibuprofen	DIPHENHYDRAMINE HCL AND IBUPROFEN	Aurohealth LLC	39af6dfa-e822-43a5-bd1a-338cf5da89ce	2022-12-09	Warnings	Exact identifier unii: WK2XYI10QM
Miranda Castros healing cell salts for bones, hair, nails and teeth Homeopathic Combination	CALCAREA FLUORICA, CALCAREA PHOSPHORICA, SILICEA	OHM PHARMA INC.	044a7174-f7a3-490f-9cad-01f2665d7575	2022-12-02	Warnings	Exact identifier unii: ETJ7Z6XBU4
Ibuprofen	IBUPROFEN	Walgreens	6bd8a0c2-314f-47cb-80cd-1d4dd92b209f	2022-11-29	Warnings	Exact identifier unii: WK2XYI10QM
Concentrated ibuprofen infants	IBUPROFEN	Guardian Drug Company	3a32f0c7-c03e-4783-a429-08280993ddfb	2022-11-28	Warnings	Exact identifier unii: WK2XYI10QM
Ibuprofen	IBUPROFEN	TOPCO ASSOCIATES LLC	cef74c2f-0c23-609d-e053-2a95a90a6b8e	2022-11-23	Warnings	Exact identifier unii: WK2XYI10QM
Ibuprofen	IBUPROFEN	Care One (American Sales Company)	016299ef-ad40-46fd-acfc-e74ffee3d9b4	2022-11-21	Warnings	Exact identifier unii: WK2XYI10QM
4 Kids Cold and Mucus Nighttime	EUPHRASIA STRICTA,SILICON DIOXIDE, RUMEX CRISPUS ROOT, ANEMONE PULSATILLA, GOLDENSEAL, SODIUM CHLORIDE, PHOSPHORUS, ONION, BRYONIA ALBA ROOT, MATRICARIA CHAMOMILLA, ARABICA COFFEE BEAN, CALCIUM SULFIDE AND SULFUR	Hyland's Inc.	6f7b2585-2f0e-5938-e053-2a91aa0aa9d1	2022-11-21	Warnings	Exact identifier unii: ETJ7Z6XBU4
4 Kids Complete Cold and Mucus	BRYONIA ALBA ROOT, EUPHRASIA STRICTA, CALCIUM SULFIDE, SODIUM CHLORIDE, PHOSPHORUS, ANEMONE PULSATILLA, RUMEX CRISPUS ROOT, AND SILICON DIOXIDE	Hyland's Inc.	ef39fe3d-a42d-4baa-9199-91f664feb432	2022-11-21	Warnings	Exact identifier unii: ETJ7Z6XBU4
signature care childrens ibuprofen	IBUPROFEN	Safeway	c30fbb8f-a293-4f6e-9495-11402548fe2d	2022-11-15	Warnings	Exact identifier unii: WK2XYI10QM
Ibuprofen	IBUPROFEN	Dolgencorp, Inc. (DOLLAR GENERAL & REXALL)	7f510feb-023c-4974-af6d-3e7a30cef362	2022-11-07	Warnings	Exact identifier unii: WK2XYI10QM
Ibuprofen	IBUPROFEN	Dolgencorp, Inc. (DOLLAR GENERAL & REXALL)	8de40427-1be3-4a86-bc4c-9659ebaa203f	2022-11-07	Warnings	Exact identifier unii: WK2XYI10QM
Ibuprofen and Pseudoephedrine HCl	IBUPROFEN AND PSEUDOEPHEDRINE HCL	Amerisource Bergen	8d397f4f-ac5e-426d-a26b-ee064b6e5028	2022-11-04	Warnings	Exact identifier unii: WK2XYI10QM
Ibuprofen	IBUPROFEN	Proficient Rx LP	9e9fb921-6b6a-422e-95b6-41d6b9047b80	2022-11-01	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: WK2XYI10QM
DG Health childrens ibuprofen	IBUPROFEN	Dolgencorp, LLC	0fd6fcca-cbfe-48af-80dd-2607b5d51b53	2022-10-13	Warnings	Exact identifier unii: WK2XYI10QM
Circle K Ibuprofen	IBUPROFEN	Lil Drug Store Products, Inc	791a7375-34b2-449b-9284-3c49a2704619	2022-10-11	Warnings	Exact identifier unii: WK2XYI10QM
Ibuprofen	IBUPROFEN	PharmPak, Inc.	b493bf76-1e8b-4e72-bef6-aca4efc69cbe	2022-10-09	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: WK2XYI10QM
Ibuprofen	IBUPROFEN	PharmPak, Inc.	4d95bccd-8280-4d03-a574-927669c7cda0	2022-10-09	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: WK2XYI10QM
Ibuprofen	IBUPROFEN	PharmPak, Inc.	bb6d0547-c113-42f9-8bf2-c227a55ab758	2022-10-09	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: WK2XYI10QM
Circle K Ibuprofen	IBUPROFEN	Lil Drug Store Products, Inc	805d9d80-7de7-49d9-afdb-3a645059fe35	2022-09-21	Warnings	Exact identifier unii: WK2XYI10QM

Reported adverse events (FAERS/openFDA)#

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