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 206 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 SODIUM TOPICAL GEL, 1%,	Asclemed USA, Inc.	988abe66-0b3b-4c13-87b4-adc913227fc5	2020-10-24	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: QTG126297Q
GUNA MATRIX DETOX	SODIUM SULFATE - PODOPHYLLUM PELTATUM ROOT - SOLIDAGO VIRGAUREA FLOWERING TOP - APIS MELLIFERA - EQUISETUM HYEMALE - STRYCHNOS NUX VOMICA SEED - HAMAMELIS VIRGINIANA ROOT BARK STEM BARK - LYCOPODIUM CLAVATUM SPORE - GALIUM APARINE WHOLE - THUJA OCCIDENTALIS LEAFY TWIG - BERBERIS VULGARIS ROOT BARK - MYOSOTIS ARVENSIS - CHELIDONIUM MAJUS WHOLE - FUCUS VESICULOSUS -	Guna spa	a369b95b-4d57-f149-e053-2995a90a87e3	2020-10-23	Warnings, Adverse reactions	Exact identifier unii: ETJ7Z6XBU4
Supreme	ABROTANUM, ANACARDIUM ORIENTALE, ARSENICUM ALBUM, BARYTA MURIATICA, HELLEBORUS NIGER, IGNATIA AMARA, LYCOPODIUM CLAVATUM, NICOTINAMIDUM, SECALE CORNUTUM, THYMUS (BOVINE), THYROIDINUM (BOVINE), CALCAREA CARBONICA, CALCAREA PHOSPHORICA, HYPOTHALAMUS SUIS, PITUITARUM POSTERIUM (BOVINE), SILICEA	BOUARI GROUP, LLC dba WEIGHT LOSS COMPANY, THE	72c4679b-aa97-4888-9178-581d0f99c0b6	2020-09-11	Warnings	Exact identifier unii: ETJ7Z6XBU4
Diclofenac Sodium	DICLOFENAC SODIUM	Proficient Rx LP	20107264-e533-4de9-9a37-59fde7981c92	2020-09-01	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: QTG126297Q
Diclofenac Sodium	DICLOFENAC SODIUM	Asclemed USA, Inc.	1e39f8d4-56a2-4d29-a971-495574e8d4a7	2020-06-17	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: QTG126297Q
Bach Original Flower Remedies	WATER	Nelson Bach USA Limited	09c76050-42c5-4403-865c-a1f6f668d9c0	2020-06-15	Warnings	Exact identifier unii: 059QF0KO0R
Diclofenac Sodium	DICLOFENAC SODIUM	Proficient Rx LP	7bc185e2-e749-4a24-8550-c2f6d39222d2	2020-04-01	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: QTG126297Q
Diclofenac sodium	DICLOFENAC SODIUM	Proficient Rx LP	b0f9e649-6651-406f-a9fe-157fe04d9d27	2020-02-01	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: QTG126297Q
Sterile Water	WATER	Baxter Healthcare Company	8bcf5572-49e1-4302-9522-56f57904cb4a	2019-12-29	Warnings, Adverse reactions	Exact identifier unii: 059QF0KO0R
Diclofenac Sodium	DICLOFENAC SODIUM	Proficient Rx LP	a7447467-79e0-436e-a273-d1ddd06169cf	2019-11-01	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: QTG126297Q
Diclofenac Sodium	DICLOFENAC SODIUM	Proficient Rx LP	77c3cb56-c071-4d92-a0d6-022417a27de4	2019-11-01	Boxed warning, Warnings, Adverse reactions	Exact identifier application number: ANDA074514 rxcui: 855926 unii: QTG126297Q
Lidocaine	LIDOCAINE	Proficient Rx LP	cbf01b82-c43f-4bed-a1df-7569f4816c76	2019-11-01	Warnings, Adverse reactions	Exact identifier unii: 98PI200987
No7 Perfect and Perfect Intense Advanced All in One Foundation SPF 50 Cool Vanilla	OCTINOXATE, TITANIUM DIOIXIDE, OCTISALATE	BCM Cosmetique SAS	d701c221-9f68-47ff-b766-2f4f1998649f	2019-10-08	Warnings	Exact identifier unii: 15FIX9V2JP
No7 Perfect and Perfect Intense Advanced All in One Foundation SPF 50 Amber	OCTINOXATE, TITANIUM DIOIXIDE, OCTISALATE	BCM Cosmetique SAS	7f5e6872-4d26-410e-8afe-16a016f9a399	2019-10-08	Warnings	Exact identifier unii: 15FIX9V2JP
No7 Perfect and Perfect Advanced All in One Foundation SPF 50 Warm Ivory	OCTINOXATE, TITANIUM DIOIXIDE, OCTISALATE	BCM Cosmetique SAS	1124ba7d-a328-409b-8c88-e74bb3e501f5	2019-10-08	Warnings	Exact identifier unii: 15FIX9V2JP
No7 Perfect and Perfect Advanced All in One Foundation SPF 50 Honey	OCTINOXATE, TITANIUM DIOIXIDE, OCTISALATE	BCM Cosmetique SAS	9c407dc7-fcde-4660-9a06-57bd8a6b867d	2019-10-08	Warnings	Exact identifier unii: 15FIX9V2JP
No7 Perfect and Perfect Intense Advanced All in One Foundation SPF 50 Chestnut	OCTINOXATE, TITANIUM DIOIXIDE, OCTISALATE	BCM Cosmetique SAS	f07e8bb2-30ae-4337-ad60-84f55f2ff354	2019-10-08	Warnings	Exact identifier unii: 15FIX9V2JP
Skin Klear Acne Relief	TRIBASIC CALCIUM PHOSPHATE, FUMARIA OFFICINALIS FLOWERING TOP, ARCTIUM LAPPA ROOT, SODIUM CHLORIDE, SAPONARIA OFFICINALIS ROOT, SILICON DIOXIDE, SOLIDAGO VIRGAUREA FLOWERING TOP, SULFUR, VIOLA TRICOLOR	Homeocare Laboratories	65afbc20-611b-4bc4-a151-c633bec66a82	2018-12-31	Warnings	Exact identifier unii: ETJ7Z6XBU4
Sinus Relief	ASAFETIDA, ECHINACEA ANGUSTIFOLIA, CALCIUM SULFIDE, POTASSIUM DICHROMATE, LUFFA OPERCULATA WHOLE, SILICON DIOXIDE, SINUSITISINUM	Homeocare Laboratories	84483171-df92-47de-9203-ed02d64fb5fb	2018-12-31	Warnings	Exact identifier unii: ETJ7Z6XBU4
Hair-X Hair Loss Relief	CADMIUM SULFATE, GRAPHITE, PHOSPHORIC ACID, SILICON DIOXIDE, SELENIUM, THALLIUM, USTILAGO MAYDIS	Homeocare Laboratories	00b62179-e03b-4972-902d-3a0c969b59bc	2018-12-31	Warnings	Exact identifier unii: ETJ7Z6XBU4

Reported adverse events (FAERS/openFDA)#

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