NDC 02282-015 - Inflammation Reduction Pack

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: 02282-015
Manufacturer: TMIG, Inc. | Actavis Elisabeth LLC | Actavis LLC | Shasun Pharmaceuticals Limited
Effective date: 2015-10-27
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Inflammation Reduction Pack - TMIG, Inc. \| Actavis Elisabeth LLC \| Actavis LLC \| Shasun Pharmaceuticals Limited	TMIG, Inc. \| Actavis Elisabeth LLC \| Actavis LLC \| Shasun Pharmaceuticals Limited	2015-10-27	HUMAN PRESCRIPTION DRUG LABEL

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
DICLOFENAC SODIUM	ACTIVE INGREDIENT	QTG126297Q	INFLAMMATION REDUCTION PACK KIT [TMIG, INC.]	3
LIDOCAINE	ACTIVE INGREDIENT	98PI200987	INFLAMMATION REDUCTION PACK KIT [TMIG, INC.]	3
PRILOCAINE	ACTIVE INGREDIENT	046O35D44R	INFLAMMATION REDUCTION PACK KIT [TMIG, INC.]	3
RANITIDINE HYDROCHLORIDE	ACTIVE INGREDIENT	BK76465IHM	INFLAMMATION REDUCTION PACK KIT [TMIG, INC.]	3
DICLOFENAC	ACTIVE MOIETY	144O8QL0L1	INFLAMMATION REDUCTION PACK KIT [TMIG, INC.]	3
LIDOCAINE	ACTIVE MOIETY	98PI200987	INFLAMMATION REDUCTION PACK KIT [TMIG, INC.]	3
PRILOCAINE	ACTIVE MOIETY	046O35D44R	INFLAMMATION REDUCTION PACK KIT [TMIG, INC.]	3
RANITIDINE	ACTIVE MOIETY	884KT10YB7	INFLAMMATION REDUCTION PACK KIT [TMIG, INC.]	3
ALUMINUM HYDROXIDE	INACTIVE INGREDIENT	5QB0T2IUN0	INFLAMMATION REDUCTION PACK KIT [TMIG, INC.]	3
CARBOMER HOMOPOLYMER TYPE B (ALLYL SUCROSE CROSSLINKED)	INACTIVE INGREDIENT	Z135WT9208	INFLAMMATION REDUCTION PACK KIT [TMIG, INC.]	3
CELLULOSE, MICROCRYSTALLINE	INACTIVE INGREDIENT	OP1R32D61U	INFLAMMATION REDUCTION PACK KIT [TMIG, INC.]	3
CROSCARMELLOSE SODIUM	INACTIVE INGREDIENT	M28OL1HH48	INFLAMMATION REDUCTION PACK KIT [TMIG, INC.]	3
FD&C RED NO. 40	INACTIVE INGREDIENT	WZB9127XOA	INFLAMMATION REDUCTION PACK KIT [TMIG, INC.]	3
FERROSOFERRIC OXIDE	INACTIVE INGREDIENT	XM0M87F357	INFLAMMATION REDUCTION PACK KIT [TMIG, INC.]	3
HYPROMELLOSES	INACTIVE INGREDIENT	3NXW29V3WO	INFLAMMATION REDUCTION PACK KIT [TMIG, INC.]	3
LACTOSE MONOHYDRATE	INACTIVE INGREDIENT	EWQ57Q8I5X	INFLAMMATION REDUCTION PACK KIT [TMIG, INC.]	3
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	INFLAMMATION REDUCTION PACK KIT [TMIG, INC.]	3
PEG-55 HYDROGENATED CASTOR OIL	INACTIVE INGREDIENT	0WZF1506N9	INFLAMMATION REDUCTION PACK KIT [TMIG, INC.]	3
POLYETHYLENE GLYCOLS	INACTIVE INGREDIENT	3WJQ0SDW1A	INFLAMMATION REDUCTION PACK KIT [TMIG, INC.]	3
POLYSORBATE 80	INACTIVE INGREDIENT	6OZP39ZG8H	INFLAMMATION REDUCTION PACK KIT [TMIG, INC.]	3
POLYVINYL ACETATE PHTHALATE	INACTIVE INGREDIENT	58QVG85GW3	INFLAMMATION REDUCTION PACK KIT [TMIG, INC.]	3
PROPYLENE GLYCOL	INACTIVE INGREDIENT	6DC9Q167V3	INFLAMMATION REDUCTION PACK KIT [TMIG, INC.]	3
SILICON DIOXIDE	INACTIVE INGREDIENT	ETJ7Z6XBU4	INFLAMMATION REDUCTION PACK KIT [TMIG, INC.]	3
SODIUM ALGINATE	INACTIVE INGREDIENT	C269C4G2ZQ	INFLAMMATION REDUCTION PACK KIT [TMIG, INC.]	3
SODIUM HYDROXIDE	INACTIVE INGREDIENT	55X04QC32I	INFLAMMATION REDUCTION PACK KIT [TMIG, INC.]	3
SODIUM STARCH GLYCOLATE TYPE A POTATO	INACTIVE INGREDIENT	5856J3G2A2	INFLAMMATION REDUCTION PACK KIT [TMIG, INC.]	3
STEARIC ACID	INACTIVE INGREDIENT	4ELV7Z65AP	INFLAMMATION REDUCTION PACK KIT [TMIG, INC.]	3
TALC	INACTIVE INGREDIENT	7SEV7J4R1U	INFLAMMATION REDUCTION PACK KIT [TMIG, INC.]	3
TITANIUM DIOXIDE	INACTIVE INGREDIENT	15FIX9V2JP	INFLAMMATION REDUCTION PACK KIT [TMIG, INC.]	3
TRIACETIN	INACTIVE INGREDIENT	XHX3C3X673	INFLAMMATION REDUCTION PACK KIT [TMIG, INC.]	3
WATER	INACTIVE INGREDIENT	059QF0KO0R	INFLAMMATION REDUCTION PACK KIT [TMIG, INC.]	3

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 199 of 210 · 4,189 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Diclofenac Sodium	DICLOFENAC	Asclemed USA, Inc.	9df599de-6412-a94e-e053-2995a90a1741	2022-10-12	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: QTG126297Q
Lidocaine	LIDOCAINE	Asclemed USA, Inc.	80dadfb5-cbe6-475f-9980-a1b255982753	2022-10-12	Warnings, Adverse reactions	Exact identifier unii: 98PI200987
Bach Original Flower Remedies Rock Water	WATER	Nelson Bach USA Limited	ea242559-1618-3354-e053-2a95a90a1a95	2022-10-03	Warnings	Exact identifier unii: 059QF0KO0R
Sterile Water	WATER	Medical Purchasing Solutions, LLC	e90b47e3-9636-b9ee-e053-2a95a90ad48c	2022-09-19	Warnings, Adverse reactions	Exact identifier unii: 059QF0KO0R
REFRESH OPTIVE Advanced	CARBOXYMETHYLCELLULOSE SODIUM, GLYCERIN, POLYSORBATE 80	Allergan, Inc.	ebd0839e-2e1d-4e0e-986c-19f1f5c76358	2022-09-15	Warnings	Exact identifier unii: 6OZP39ZG8H
Diclofenac sodium	DICLOFENAC SODIUM	Asclemed USA, Inc.	d4b81a74-6926-4715-bf90-aec026cff2b4	2022-09-09	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: QTG126297Q
REFRESH OPTIVE Advanced	CARBOXYMETHYLCELLULOSE SODIUM, GLYCERIN, AND POLYSORBATE 80	Allergan, Inc.	aaa943e4-7c38-4c5a-b7c0-5a656d8cafc0	2022-09-01	Warnings	Exact identifier unii: 6OZP39ZG8H
Diclofenac Sodium	DICLOFENAC SODIUM	Asclemed USA, Inc.	b162d65d-b105-4a68-90bb-316b9686267b	2022-08-24	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: QTG126297Q
Diclofenac Sodium	DICLOFENAC SODIUM	Rite Aid Corporation	1c9ea3b2-8f45-420b-87d3-dc7de0be2d5f	2022-08-23	Warnings	Exact identifier unii: QTG126297Q
Hendel Periodontal and Tooth Pain Relief	SODIUM BORATE, TRIBASIC CALCIUM PHOSPHATE, MERCURIUS SOLUBILIS, AND SILICON DIOXIDE	MediNatura Inc	f34e9f77-69fd-4c7f-9eea-2d721a4d27fb	2022-08-22	Warnings	Exact identifier unii: ETJ7Z6XBU4
diclofenac sodium	DICLOFENAC SODIUM	Proficient Rx LP	67e384c6-8476-4aad-b967-241335538d56	2022-08-01	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: QTG126297Q
Diclofenac Sodium Delayed Release	DICLOFENAC SODIUM	Proficient Rx LP	afce2de2-0c59-4191-bf79-782ca31e427d	2022-07-01	Boxed warning, Warnings, Adverse reactions	Exact identifier rxcui: 855926 unii: QTG126297Q
Diclofenac Sodium Misoprostol	DICLOFENAC SODIUM AND MISOPROSTOL	Proficient Rx LP	33f7db0b-f049-4d2e-abf5-4db97222e175	2022-07-01	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: QTG126297Q
REFRESH Optive Mega-3	CARBOXYMETHYLCELLULOSE SODIUM, GLYCERIN AND POLYSORBATE 80	Allergan, Inc.	c5f2b3f2-2071-45bd-a010-67f848bc0233	2022-06-30	Warnings	Exact identifier unii: 6OZP39ZG8H
Sterile Water	WATER	Fresenius Kabi USA, LLC	f42ac50f-0ec5-4713-a4c8-99d972d90bed	2022-06-22	Warnings, Adverse reactions	Exact identifier unii: 059QF0KO0R
Sterile Water	WATER	Fresenius Kabi USA, LLC	e71c6c83-d518-496c-b2ab-efd5987e4783	2022-06-09	Warnings, Adverse reactions	Exact identifier unii: 059QF0KO0R
Diclofenac Sodium	DICLOFENAC SODIUM	A-S Medication Solutions	3a520306-fe3e-4830-963f-04b080db3abc	2022-06-01	Warnings, Adverse reactions	Exact identifier unii: QTG126297Q
good sense arthritis pain	DICLOFENAC SODIUM	Proficient Rx LP	67eacd91-8378-47e7-9bad-1e7b685aa9d4	2022-06-01	Warnings	Exact identifier unii: QTG126297Q
Addiclenz	BETA VULGARIS, BOLDO, CHELIDONIUM MAJUS, PETROSELINUM SATIVUM, TARAXACUM OFFICINALE, ARSENICUM ALBUM, BISPHENOL A, COBALTUM METALLICUM, CUPRUM METALLICUM, GLYPHOSATE, IODIUM, LYCOPODIUM CLAVATUM, PHOSPHORICUM ACIDUM, SELENIUM METALLICUM, ZINCUM METALLICUM, ASPARTAME, BENZALKONIUM CHLORIDE, FORMALINUM, METHYLENE CHLORIDE, METHYL PARABEN, PROPYL PARABEN, SODIUM BENZOATE, SODIUM CITRATE, TITANIUM DIOXIDE, ZINCUM OXYDATUM	Deseret Biologicals, Inc.	e39235ea-2a2f-44a7-92d6-fb1d428ebabd	2022-05-12	Warnings	Exact identifier unii: 15FIX9V2JP
Blockaid	LIDOCAINE, TETRACAINE	SofTap Inc	de3af3fa-8acf-2379-e053-2995a90ac77d	2022-05-06	Warnings	Exact identifier unii: 98PI200987

Reported adverse events (FAERS/openFDA)#

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