NDC 05912-017 - 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: 05912-017
Package NDCs from labels: 05912-017-60
Manufacturer: TMIG, Inc. | Actavis Elisabeth LLC | Actavis LLC | Shasun Pharmaceuticals Limited
Effective date: 2015-11-18
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Emla Cream - TMIG, Inc. \| Actavis Elisabeth LLC \| Actavis LLC \| Shasun Pharmaceuticals Limited	TMIG, Inc. \| Actavis Elisabeth LLC \| Actavis LLC \| Shasun Pharmaceuticals Limited	2015-11-18	HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
05912-017-60	Inflammation Reduction Pack	60 g in 1 TUBE	CREAM	60 g	25 mg in 1g	4

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
05912-017	INFLAMMATION REDUCTION PACK KIT [TMIG, INC.]	4	Unmatched	20151119_f7f3dcf8-8628-467f-b195-d2dd7e11ae93.zip

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

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 50 of 214 · 4,279 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Dior Forever Skin Wear Flawless Skin True Foundation SPF 20 4W Warm	OCTISALATE, TITANIUM DIOXIDE	Parfums Christian Dior	58efeaaf-d3c6-44e9-b60f-8f22f5bb1d33	2026-01-16	Warnings	Exact identifier unii: 15FIX9V2JP
Dior Forever Skin Wear Flawless Skin True Foundation SPF 20 4WP Warm Peach	OCTISALATE, TITANIUM DIOXIDE	Parfums Christian Dior	f6b4a90b-5905-4f62-9e35-f2b1dda8dddd	2026-01-16	Warnings	Exact identifier unii: 15FIX9V2JP
Berberis Quartz	BERBERIS QUARTZ	Uriel Pharmacy Inc.	5da48d70-1140-495d-b672-0e55c04196e1	2026-01-16	Warnings	Exact identifier unii: ETJ7Z6XBU4
BRUSH and GO SPF 50 ALL SKIN TYPES BROAD SPECTRUM	TITANIUM DIOXIDE, OCTINOXATE, OCTOCRYLENE, OCTISALATE, AVOBENZONE, AND OXYBENZONE	Noon Aesthetics M.R. Ltd	0d9f132c-7630-4261-a0f8-fc7a4377731f	2026-01-16	Warnings	Exact identifier unii: 15FIX9V2JP
BRUSH and GO SPF 50 OILY/PROBLEMATIC SKIN BROAD SPECTRUM	TITANIUM DIOXIDE, OCTINOXATE, OCTOCRYLENE, OCTISALATE, AVOBENZONE, AND OXYBENZONE	Noon Aesthetics M.R. Ltd	f292da7d-ffd2-41c3-9a64-619aab19ff18	2026-01-15	Warnings	Exact identifier unii: 15FIX9V2JP
Aspercreme with Lidocaine XL	LIDOCAINE	Chattem, Inc.	b0859b10-539e-4905-ab52-af78b778d6a4	2026-01-15	Warnings	Exact identifier unii: 98PI200987
ARTHRITIS PAIN RELIEVER	DICLOFENAC SODIUM	Publix Super Markets Inc	bae07276-c800-468e-a201-e6268846fff3	2026-01-15	Warnings	Exact identifier unii: QTG126297Q
Multivit Sun Protector	TITANIUM DIOXIDE, OCTOCRYLENE, AND AVOBENZONE	Noon Aesthetics M.R. Ltd	abdb560d-29be-41dc-ad23-54ea571acb14	2026-01-15	Warnings	Exact identifier unii: 15FIX9V2JP
Pain Relieving Patch	LIDOCAINE	FlexiGo Inc.	4868af2a-c4be-9c68-e063-6394a90a565b	2026-01-15	Warnings	Exact identifier unii: 98PI200987
Hemorrhoid and Fissure	GLYCERIN 6%,LIDOCAINE 4%,ECTOIN 0.12%	FlexiGo Inc	48697377-61c0-1b0a-e063-6294a90a3293	2026-01-15	Warnings	Exact identifier unii: 98PI200987
Careland Lidocaine 4 Pain Relieving Gel-Patches	LIDOCAINE	Planet (Anhui) Pharmaceutical Co., Ltd.	a6ca8382-7ce5-4df9-912e-8a0ac0423116	2026-01-15	Warnings	Exact identifier unii: 98PI200987
Diclofenac Sodium	DICLOFENAC SODIUM	A-S Medication Solutions	47793dca-5e9e-44ee-8e66-5e42e1831b1e	2026-01-15	Boxed warning, Warnings, Adverse reactions	Exact identifier application number: ANDA074514 rxcui: 855926 unii: QTG126297Q
Icy Hot Lidocaine Dry	LIDOCAINE, MENTHOL	Chattem, Inc.	d500a74e-ab93-4919-8665-a89e9d4cad28	2026-01-15	Warnings	Exact identifier unii: 98PI200987
Diclofenac Sodium	DICLOFENAC SODIUM	A-S Medication Solutions	b74be49d-74ff-491b-962b-0edd3a57cbc9	2026-01-15	Boxed warning, Warnings, Adverse reactions	Exact identifier application number: ANDA074514 unii: QTG126297Q
DICLOFENAC SODIUM TOPICAL	DICLOFENAC SODIUM	CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED	181e32ab-5ec0-4be4-bad0-b6bbafc08f85	2026-01-15	Warnings	Exact identifier unii: QTG126297Q
Diclofenac Sodium	DICLOFENAC SODIUM	Sportpharm LLC	929f71ab-f0c8-4331-800d-ed4a172e647e	2026-01-14	Warnings	Exact identifier unii: QTG126297Q
Diclofenac sodium	DICLOFENAC SODIUM	Sportpharm LLC	ac631742-119f-408a-8b36-b041bab743e2	2026-01-14	Warnings	Exact identifier unii: QTG126297Q
LIDOCORE (single unit patch)	LIDOCAINE 4%	Ion Pharma, LLC	161f5745-fec1-4ca3-be42-512f6d3e7fee	2026-01-14	Warnings	Exact identifier unii: 98PI200987
LIDOCORE	LIDOCAINE 4%	Ion Pharma, LLC	12dec398-1082-45ad-a517-8f12873b1909	2026-01-14	Warnings	Exact identifier unii: 98PI200987
Diclofenac Sodium	DICLOFENAC SODIUM	AvKARE	19b4ff5c-adb7-a0d0-7ef2-4ae05047fd94	2026-01-14	Boxed warning, Warnings, Adverse reactions	Exact identifier rxcui: 855926 unii: QTG126297Q

Reported adverse events (FAERS/openFDA)#

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