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 165 of 211 · 4,219 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Mind Detox and Drainage	ALUMINA, BARYTA CARBONICA, CARBONEUM SULPHURATUM, CEREBRUM SUIS, CONIUM MACULATUM, HELLEBORUS NIGER, LECITHIN, LYCOPODIUM CLAVATUM, MANDRAGORA OFFICINARUM, MERCURIUS SOLUBILIS, NAJA TRIPUDIANS, PICRICUM ACIDUM, PLATINUM METALLICUM, SILICEA, STRAMONIUM, SULPHURICUM ACIDUM, ZINCUM PHOSPHORATUM	Deseret Biologicals, Inc.	1ac1e955-a374-4cac-b997-51c6aef8d35d	2024-08-01	Warnings	Exact identifier unii: ETJ7Z6XBU4
Essential Sheer SPF 50	ZINC OXIDE TITANIUM DIOXIDE	Topiderm, Inc.	2132dc18-85ee-4449-86d2-d9f698f286c6	2024-07-31	Warnings	Exact identifier unii: 15FIX9V2JP
diclofenac sodium	DICLOFENAC SODIUM	Padagis Israel Pharmaceuticals Ltd	3f0f3514-c3f7-4dab-8e5f-ddf89adbe3b8	2024-07-31	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: QTG126297Q
Proceuticals Private Label by TiZO tinted foaming mineral sunscreen	TITANIUM DIOXIDE, ZINC OXIDE	Fallien Cosmeceuticals, Ltd	1e78109f-4d2e-2705-e063-6294a90a5ad3	2024-07-30	Warnings	Exact identifier unii: 15FIX9V2JP
Replenix Sheer SPF 50	ZINC OXIDE TITANIUM DIOXIDE	Topiderm, Inc.	37d1f454-3bc9-4ce5-863c-0d4f6fa18fb4	2024-07-29	Warnings	Exact identifier unii: 15FIX9V2JP
Diclofenac Sodium	DICLOFENAC SODIUM	NuCare Pharmaceuticals,Inc.	005299ac-b6de-511f-e063-6294a90a29e0	2024-07-29	Warnings	Exact identifier unii: QTG126297Q
Fruit of the Earth Aloe Vera Cool Blue	LIDOCAINE HYDROCHLORIDE	Fruit of the Earth, Inc.	1d65bc34-2bc2-4f52-a9b3-1cb08324eb79	2024-07-19	Warnings	Exact identifier unii: 98PI200987
Diclofenac Sodium Delayed Release	DICLOFENAC SODIUM	NuCare Pharmaceuticals, Inc.	4b44ac98-225c-1739-e054-00144ff88e88	2024-07-19	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: QTG126297Q
Diclofenac Sodium	DICLOFENAC SODIUM	NuCare Pharmaceuticals,Inc.	abacf60f-0410-e6da-e053-2995a90a413c	2024-07-17	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: QTG126297Q
Derma E Sun Defense Face SPF 30	ZINC OXIDE TITANIUM DIOXIDE	derma e	d90b8f81-de7a-4022-800a-90f063e94180	2024-07-17	Warnings	Exact identifier unii: 15FIX9V2JP
PROCEUTICALS PRIVATE LABEL by TiZO mineral lip sunscreen	TITANIUM DIOXIDE, ZINC OXIDE	Fallien Cosmeceuticals, LTD	1d611494-648b-6e5f-e063-6294a90a4500	2024-07-16	Warnings	Exact identifier unii: 15FIX9V2JP
Diclofenac Sodium	DICLOFENAC	Amneal Pharmaceuticals LLC	78873f83-cea9-44d4-8ad4-8cb9257e5c7f	2024-07-16	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: QTG126297Q
SkinCeuticals Physical Fusion UV Defense Broad Spectrum SPF 50 Sunscreen	TITANIUM DIOXIDE AND ZINC OXIDE	L'Oreal USA Products Inc	8df98d97-a5d2-4d52-8bd2-130a13501d60	2024-07-16	Warnings	Exact identifier unii: 15FIX9V2JP
Lidocaine and Prilocaine	LIDOCAINE AND PRILOCAINE	NuCare Pharamceuticals,Inc.	5900691d-8b50-7752-e053-2991aa0a5c5c	2024-07-15	Warnings, Adverse reactions	Exact identifier rxcui: 197877 unii: 98PI200987 unii: 046O35D44R
Tidl Pain Relief Evening Therapy Spray.	PAIN RELIEF EVENING THERAPY SPRAY	Shenzhen Sam Technology Co., Ltd.	1d1a2f4a-7b25-e595-e063-6394a90a00d5	2024-07-13	Warnings	Exact identifier unii: 98PI200987
TIDL PAIN RELIEF HEAT THERAPY ROLL-ON	PAIN RELIEF HEAT THERAPY ROLL-ON	Shenzhen Sam Technology Co., Ltd.	1d0b7b8f-9e5d-00f7-e063-6394a90af87c	2024-07-12	Warnings	Exact identifier unii: 98PI200987
Thompson Safety Eyewash	WATER	Thompson Safety	1d0e96cf-245b-cfb7-e063-6294a90a4ced	2024-07-12	Warnings	Exact identifier unii: 059QF0KO0R
TIDL PAIN RELIEF HEAT THERAPY Spray.	PAIN RELIEF HEAT THERAPY SPRAY	Shenzhen Sam Technology Co., Ltd.	1d199826-1b27-b6e7-e063-6394a90a69ad	2024-07-12	Warnings	Exact identifier unii: 98PI200987
Derma E Sun Defense SPF 30	ZINC OXIDE AND TITANIUM DIOXIDE	derma e	395b73a4-dae7-49da-9dab-ab622117c8c0	2024-07-12	Warnings	Exact identifier unii: 15FIX9V2JP
Diclofenac sodium	DICLOFENAC SODIUM	Advanced Rx of Tennessee, LLC	1d4d6370-2b45-fa6d-e063-6294a90a4a67	2024-07-11	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: QTG126297Q

Reported adverse events (FAERS/openFDA)#

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