NDC 0781-1883-13 - 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: 0781-1883
Requested NDC: 0781-1883-13
Package NDCs from labels: 0781-1883-13
Manufacturer: TMIG, Inc. | EPM Packaging | Garcoa, Inc. | Sandoz Inc. | Actavis Elizabeth LLC
Effective date: 2015-08-18
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Inflamation Reduction Pack	TMIG, Inc. \| EPM Packaging \| Garcoa, Inc. \| Sandoz Inc. \| Actavis Elizabeth LLC	2015-08-18	HUMAN PRESCRIPTION DRUG LABEL
Ranitidine Hydrochloride - Keltman Pharmaceuticals Inc. \| Sandhills Packaging	Keltman Pharmaceuticals Inc. \| Sandhills Packaging	2010-06-03	HUMAN PRESCRIPTION DRUG LABEL
Ranitidine Hydrochloride - State of Florida DOH Central Pharmacy	State of Florida DOH Central Pharmacy	2010-04-13	HUMAN PRESCRIPTION DRUG LABEL
National Council for Prescription Drug Programs indexing - billing unit	National Council for Prescription Drug Programs	2012-07-24	Indexing - Billing Unit

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Related label table
NDC	Effective	Related label
0781-1883-01	2020-08-19	Ranitidine Hydrochloride Capsules Rx Only
0781-1883-05	2020-08-19	Ranitidine Hydrochloride Capsules Rx Only
0781-1883-10	2020-08-19	Ranitidine Hydrochloride Capsules Rx Only
0781-1883-60	2020-08-19	Ranitidine Hydrochloride Capsules Rx Only
0781-1883-01	2020-07-22	Ranitidine Hydrochloride Capsules Rx Only
0781-1883-05	2020-07-22	Ranitidine Hydrochloride Capsules Rx Only
0781-1883-10	2020-07-22	Ranitidine Hydrochloride Capsules Rx Only
0781-1883-60	2020-07-22	Ranitidine Hydrochloride Capsules Rx Only

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
0781-1883-10	EA - Each	0781-1883	e49cab76-efcd-43e8-9091-65805c64dc7d	1	2012-07-24
0781-1883-13	EA - Each	0781-1883	2b8c1983-7322-49dd-b8cc-70d37a05dd5d	1	2012-07-24
0781-1883-60	EA - Each	0781-1883	e2f0f7c7-ba64-4075-8226-76a5f41e3b9f	1	2012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
CAPSAICIN	ACTIVE INGREDIENT	S07O44R1ZM	INFLAMMATION REDUCTION PACK KIT [TMIG, INC.]	2
DICLOFENAC SODIUM	ACTIVE INGREDIENT	QTG126297Q	INFLAMMATION REDUCTION PACK KIT [TMIG, INC.]	2
RANITIDINE HYDROCHLORIDE	ACTIVE INGREDIENT	BK76465IHM	INFLAMMATION REDUCTION PACK KIT [TMIG, INC.]	2
CAPSAICIN	ACTIVE MOIETY	S07O44R1ZM	INFLAMMATION REDUCTION PACK KIT [TMIG, INC.]	2
DICLOFENAC	ACTIVE MOIETY	144O8QL0L1	INFLAMMATION REDUCTION PACK KIT [TMIG, INC.]	2
RANITIDINE	ACTIVE MOIETY	884KT10YB7	INFLAMMATION REDUCTION PACK KIT [TMIG, INC.]	2
CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED)	INACTIVE INGREDIENT	71DD5V995L	INFLAMMATION REDUCTION PACK KIT [TMIG, INC.]	2
CELLULOSE, MICROCRYSTALLINE	INACTIVE INGREDIENT	OP1R32D61U	INFLAMMATION REDUCTION PACK KIT [TMIG, INC.]	2
CETYL ACETATE	INACTIVE INGREDIENT	4Q43814HXS	INFLAMMATION REDUCTION PACK KIT [TMIG, INC.]	2
D&C RED NO. 30	INACTIVE INGREDIENT	2S42T2808B	INFLAMMATION REDUCTION PACK KIT [TMIG, INC.]	2
FERROSOFERRIC OXIDE	INACTIVE INGREDIENT	XM0M87F357	INFLAMMATION REDUCTION PACK KIT [TMIG, INC.]	2
HYDROXYPROPYL CELLULOSE (TYPE H)	INACTIVE INGREDIENT	RFW2ET671P	INFLAMMATION REDUCTION PACK KIT [TMIG, INC.]	2
HYPROMELLOSE 2910 (3 MPA.S)	INACTIVE INGREDIENT	0VUT3PMY82	INFLAMMATION REDUCTION PACK KIT [TMIG, INC.]	2
HYPROMELLOSES	INACTIVE INGREDIENT	3NXW29V3WO	INFLAMMATION REDUCTION PACK KIT [TMIG, INC.]	2
LACTOSE MONOHYDRATE	INACTIVE INGREDIENT	EWQ57Q8I5X	INFLAMMATION REDUCTION PACK KIT [TMIG, INC.]	2
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	INFLAMMATION REDUCTION PACK KIT [TMIG, INC.]	2
METHYLPARABEN	INACTIVE INGREDIENT	A2I8C7HI9T	INFLAMMATION REDUCTION PACK KIT [TMIG, INC.]	2
PEPPERMINT	INACTIVE INGREDIENT	V95R5KMY2B	INFLAMMATION REDUCTION PACK KIT [TMIG, INC.]	2
POLYETHYLENE GLYCOLS	INACTIVE INGREDIENT	3WJQ0SDW1A	INFLAMMATION REDUCTION PACK KIT [TMIG, INC.]	2
POLYSORBATE 80	INACTIVE INGREDIENT	6OZP39ZG8H	INFLAMMATION REDUCTION PACK KIT [TMIG, INC.]	2
PPG-20 METHYL GLUCOSE ETHER DISTEARATE	INACTIVE INGREDIENT	0057334FAB	INFLAMMATION REDUCTION PACK KIT [TMIG, INC.]	2
PROPYLENE GLYCOL	INACTIVE INGREDIENT	6DC9Q167V3	INFLAMMATION REDUCTION PACK KIT [TMIG, INC.]	2
PROPYLPARABEN	INACTIVE INGREDIENT	Z8IX2SC1OH	INFLAMMATION REDUCTION PACK KIT [TMIG, INC.]	2
SILICON DIOXIDE	INACTIVE INGREDIENT	ETJ7Z6XBU4	INFLAMMATION REDUCTION PACK KIT [TMIG, INC.]	2
SODIUM ALGINATE	INACTIVE INGREDIENT	C269C4G2ZQ	INFLAMMATION REDUCTION PACK KIT [TMIG, INC.]	2
SODIUM STARCH GLYCOLATE TYPE A POTATO	INACTIVE INGREDIENT	5856J3G2A2	INFLAMMATION REDUCTION PACK KIT [TMIG, INC.]	2
STEARETH-100	INACTIVE INGREDIENT	4OH5W9UM87	INFLAMMATION REDUCTION PACK KIT [TMIG, INC.]	2
STEARIC ACID	INACTIVE INGREDIENT	4ELV7Z65AP	INFLAMMATION REDUCTION PACK KIT [TMIG, INC.]	2
STEARYL ALCOHOL	INACTIVE INGREDIENT	2KR89I4H1Y	INFLAMMATION REDUCTION PACK KIT [TMIG, INC.]	2
TALC	INACTIVE INGREDIENT	7SEV7J4R1U	INFLAMMATION REDUCTION PACK KIT [TMIG, INC.]	2
TITANIUM DIOXIDE	INACTIVE INGREDIENT	15FIX9V2JP	INFLAMMATION REDUCTION PACK KIT [TMIG, INC.]	2
TRIETHYL CITRATE	INACTIVE INGREDIENT	8Z96QXD6UM	INFLAMMATION REDUCTION PACK KIT [TMIG, INC.]	2
TROLAMINE	INACTIVE INGREDIENT	9O3K93S3TK	INFLAMMATION REDUCTION PACK KIT [TMIG, INC.]	2
WATER	INACTIVE INGREDIENT	059QF0KO0R	INFLAMMATION REDUCTION PACK KIT [TMIG, INC.]	2
RANITIDINE HYDROCHLORIDE	ACTIVE INGREDIENT	BK76465IHM	RANITIDINE HYDROCHLORIDE TABLET, FILM COATED [KELTMAN PHARMACEUTICALS INC.]	1
RANITIDINE HYDROCHLORIDE	ACTIVE INGREDIENT	BK76465IHM	RANITIDINE HYDROCHLORIDE TABLET, FILM COATED [STATE OF FLORIDA DOH CENTRAL PHARMACY]	1
RANITIDINE	ACTIVE MOIETY	884KT10YB7	RANITIDINE HYDROCHLORIDE TABLET, FILM COATED [KELTMAN PHARMACEUTICALS INC.]	1
RANITIDINE	ACTIVE MOIETY	884KT10YB7	RANITIDINE HYDROCHLORIDE TABLET, FILM COATED [STATE OF FLORIDA DOH CENTRAL PHARMACY]	1
CELLULOSE, MICROCRYSTALLINE	INACTIVE INGREDIENT	OP1R32D61U	RANITIDINE HYDROCHLORIDE TABLET, FILM COATED [KELTMAN PHARMACEUTICALS INC.]	1
CELLULOSE, MICROCRYSTALLINE	INACTIVE INGREDIENT	OP1R32D61U	RANITIDINE HYDROCHLORIDE TABLET, FILM COATED [STATE OF FLORIDA DOH CENTRAL PHARMACY]	1
D&C RED NO. 30	INACTIVE INGREDIENT	2S42T2808B	RANITIDINE HYDROCHLORIDE TABLET, FILM COATED [KELTMAN PHARMACEUTICALS INC.]	1
D&C RED NO. 30	INACTIVE INGREDIENT	2S42T2808B	RANITIDINE HYDROCHLORIDE TABLET, FILM COATED [STATE OF FLORIDA DOH CENTRAL PHARMACY]	1
HYDROXYPROPYL CELLULOSE	INACTIVE INGREDIENT	RFW2ET671P	RANITIDINE HYDROCHLORIDE TABLET, FILM COATED [STATE OF FLORIDA DOH CENTRAL PHARMACY]	1
HYDROXYPROPYL CELLULOSE	INACTIVE INGREDIENT	RFW2ET671P	RANITIDINE HYDROCHLORIDE TABLET, FILM COATED [KELTMAN PHARMACEUTICALS INC.]	1
HYPROMELLOSE 2910 (3 CPS)	INACTIVE INGREDIENT	0VUT3PMY82	RANITIDINE HYDROCHLORIDE TABLET, FILM COATED [KELTMAN PHARMACEUTICALS INC.]	1
HYPROMELLOSE 2910 (3 CPS)	INACTIVE INGREDIENT	0VUT3PMY82	RANITIDINE HYDROCHLORIDE TABLET, FILM COATED [STATE OF FLORIDA DOH CENTRAL PHARMACY]	1
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	RANITIDINE HYDROCHLORIDE TABLET, FILM COATED [STATE OF FLORIDA DOH CENTRAL PHARMACY]	1
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	RANITIDINE HYDROCHLORIDE TABLET, FILM COATED [KELTMAN PHARMACEUTICALS INC.]	1
PEPPERMINT	INACTIVE INGREDIENT	V95R5KMY2B	RANITIDINE HYDROCHLORIDE TABLET, FILM COATED [KELTMAN PHARMACEUTICALS INC.]	1
PEPPERMINT	INACTIVE INGREDIENT	V95R5KMY2B	RANITIDINE HYDROCHLORIDE TABLET, FILM COATED [STATE OF FLORIDA DOH CENTRAL PHARMACY]	1
SODIUM STARCH GLYCOLATE TYPE A POTATO	INACTIVE INGREDIENT	5856J3G2A2	RANITIDINE HYDROCHLORIDE TABLET, FILM COATED [STATE OF FLORIDA DOH CENTRAL PHARMACY]	1
SODIUM STARCH GLYCOLATE TYPE A POTATO	INACTIVE INGREDIENT	5856J3G2A2	RANITIDINE HYDROCHLORIDE TABLET, FILM COATED [KELTMAN PHARMACEUTICALS INC.]	1
TITANIUM DIOXIDE	INACTIVE INGREDIENT	15FIX9V2JP	RANITIDINE HYDROCHLORIDE TABLET, FILM COATED [STATE OF FLORIDA DOH CENTRAL PHARMACY]	1
TITANIUM DIOXIDE	INACTIVE INGREDIENT	15FIX9V2JP	RANITIDINE HYDROCHLORIDE TABLET, FILM COATED [KELTMAN PHARMACEUTICALS INC.]	1
TRIETHYL CITRATE	INACTIVE INGREDIENT	8Z96QXD6UM	RANITIDINE HYDROCHLORIDE TABLET, FILM COATED [KELTMAN PHARMACEUTICALS INC.]	1
TRIETHYL CITRATE	INACTIVE INGREDIENT	8Z96QXD6UM	RANITIDINE HYDROCHLORIDE TABLET, FILM COATED [STATE OF FLORIDA DOH CENTRAL PHARMACY]	1

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 2 of 314 · 6,262 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Diclofenac Sodium	DICLOFENAC SODIUM	A-S Medication Solutions	d9698809-4887-4514-aa28-0066355ef908	2026-09-02	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: QTG126297Q
DICLOFENAC SODIUM	DICLOFENAC SODIUM	NuCare Pharmaceuticals, Inc.	5a852412-69af-6502-e063-6294a90a0748	2026-09-02	Boxed warning, Warnings, Adverse reactions	Exact identifier rxcui: 855906 unii: QTG126297Q
Diclofenac	DICLOFENAC SODIUM	YYBA CORP	533653e8-93d5-9080-e063-6394a90a165b	2026-09-01	Warnings	Exact identifier unii: QTG126297Q
Gaimoa Lidocaine Pain Relief Gel Patches	LIDOCAINE PAIN RELIEF GEL PATCHES	Henan Enokon Medical Instrument Co., Ltd.	5a68fe67-5c15-af9a-e063-6294a90a7ec1	2026-09-01	Warnings	Exact identifier application number: M017
CVS Cortisone Liquid	HYDROCORTISONE	CVS Pharmacy	42df45a9-d449-090a-e063-6394a90a9ee4	2026-09-01	Warnings	Exact identifier application number: M017
Ramedica Herbal Wonder Balm	CAMPHOR, MENTHOL	Ramedicare Sdn. Bhd.	cfb2ea0e-a1f6-4fdf-b866-346bbe78788f	2026-09-01	Warnings	Exact identifier application number: M017
La Vaquita New Regular	METHYL SALICYLATE	Delon Laboratories (1990) Ltd	d62186ac-afbb-443e-98c2-f0d122422a3c	2026-09-01	Warnings	Exact identifier application number: M017
ActivICE	MENTHOL	Medline Industries, LP	834adeb9-38ad-0cfe-e053-2991aa0af82f	2026-09-01	Warnings	Exact identifier application number: M017
La Vaquita New Extra	METHYL SALICYLATE, MENTHOL	Delon Laboratories (1990) Ltd	3097a01b-cee5-492f-b65a-63992fb28e3a	2026-09-01	Warnings	Exact identifier application number: M017
Terramed Just Think Comfort Hydrocortisone 1% Cream	HYDROCORTISONE	Rida LLC	0d2c0c2c-370f-4adb-b0ea-1e218c927f8b	2026-09-01	Warnings	Exact identifier application number: M017
Diclofenac sodium and Misoprostol	DICLOFENAC SODIUM AND MISOPROSTOL	Mylan Pharmaceuticals Inc.	a7701e8c-4e16-4165-8b83-de2c08d5ded3	2026-08-31	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: QTG126297Q
BMNP Silicea	SILICEA	Total Operations Management LLC DBA:Bestmade Natural Products Micro	5a58454f-aed6-24ba-e063-6294a90a47fb	2026-08-31	Warnings	Exact identifier unii: ETJ7Z6XBU4
Diclofenac Sodium and Misoprostol	DICLOFENAC SODIUM AND MISOPROSTOL	Actavis Pharma, Inc.	df8b8660-0c24-4848-8bea-c1b935090c66	2026-08-31	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: QTG126297Q
Itch Stopping	DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE	HyVee Inc	53157137-b980-45d2-aa10-8c111c0ec2f4	2026-08-31	Warnings	Exact identifier application number: M017
EAYONYUMT NECK PAIN RELIEF	MENTHOL	Wuhan Ruihengjie Technology Co., Ltd.	5a450e68-07a7-a4bb-e063-6294a90a97c9	2026-08-30	Warnings	Exact identifier application number: M017
EAYONYUM BACK PAIN RELIEVING	MENTHOL	Wuhan Ruihengjie Technology Co., Ltd.	5a458280-4f9c-5af6-e063-6394a90acb2e	2026-08-30	Warnings	Exact identifier application number: M017
EAYONYUM KNEE PAIN RELIEVING	MENTHOL	Wuhan Ruihengjie Technology Co., Ltd.	5a45d19f-c753-71eb-e063-6294a90a4805	2026-08-30	Warnings	Exact identifier application number: M017
Good Neighbor Pharmacy Hydrocortisone With Aloe for Sensitive Skin	HYDROCORTISONE	AmerisourceBergen	c5c5b5ca-b4d4-4fa8-b647-b3ccb2966495	2026-08-30	Warnings	Exact identifier application number: M017
Olu Pain Management	LIDOCAINE AND CAMPHOR	HAWAII REPACK, INC.	31ed3d82-ba12-46b2-b0ec-7e5e019efc10	2026-08-28	Warnings	Exact identifier application number: M017
4% Lidocaine Patches	4% LIDOCAINE PATCHES	Shenzhen Chaoxiji Technology Co.,Ltd.	5a177987-7c05-f07f-e063-6394a90aa9ba	2026-08-28	Warnings	Exact identifier application number: M017

Reported adverse events (FAERS/openFDA)#

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