NDC 35781-0500 - WPR Plus

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: 35781-0500
Package NDCs from labels: 35781-0500-3, 35781-0500-1, 35781-0500-9
Manufacturer: International Brand Management, LLC | Gensco Laboratories, LLC
Effective date: 2018-07-17
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
WPR Plus - International Brand Management, LLC \| Gensco Laboratories, LLC	International Brand Management, LLC \| Gensco Laboratories, LLC	2018-07-17	HUMAN PRESCRIPTION DRUG LABEL
WPR Plus - International Brand Management, LLC	International Brand Management, LLC	2018-07-17	HUMAN OTC DRUG LABEL
Lidocaine Hydrochloride - Gensco Laboratories, LLC	Gensco Laboratories, LLC	2015-10-01	HUMAN PRESCRIPTION DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
35781-0500-1	2020-01-31	C162847	48780-1	9d75b9d0-d18c-f424-e053-dadaa90a57ce	LDO Plus (Lidocaine HCl USP) 4%
35781-0500-3	2020-01-31	C162847	48780-1	9d75b9d0-d18c-f424-e053-dadaa90a57ce	LDO Plus (Lidocaine HCl USP) 4%
35781-0500-9	2020-01-31	C162847	48780-1	9d75b9d0-d18c-f424-e053-dadaa90a57ce	LDO Plus (Lidocaine HCl USP) 4%

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
35781-0500-3	WPR Plus	30 g in 1 TUBE		30 g	40 mg in 1g	2
35781-0500-1	Lidocaine Hydrochloride	15 g in 1 TUBE	GEL	15		1
35781-0500-1	Lidocaine Hydrochloride	1 in 1 CARTON	GEL	1		1
35781-0500-3	WPR Plus	30 g in 1 TUBE		30 g	40 mg in 1g	1
35781-0500-3	Lidocaine Hydrochloride	1 in 1 CARTON	GEL	1		1
35781-0500-3	Lidocaine Hydrochloride	30 g in 1 TUBE	GEL	30		1
35781-0500-9	Lidocaine Hydrochloride	1 in 1 CARTON	GEL	1		1
35781-0500-9	Lidocaine Hydrochloride	90 g in 1 TUBE	GEL	90		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
35781-0500	WPR PLUS () KIT [INTERNATIONAL BRAND MANAGEMENT, LLC]	2	Unmatched	20180801_9d830535-2202-482d-9d1a-bccd7bbba855.zip
35781-0500	LIDOCAINE HYDROCHLORIDE (LIDOCAINE) GEL [GENSCO LABORATORIES, LLC]	1	6 package rows	20151028_88dbd438-02c0-481a-bdb7-8b3f3c41fd46.zip
35781-0500	WPR PLUS () KIT [INTERNATIONAL BRAND MANAGEMENT, LLC]	1	Unmatched	20180717_793d6fad-31a7-4b28-8395-73825bc18508.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
35781-0500-3	ML - Milliliter	35781-0500	e34c830a-ebae-4476-af71-631a4ac662bc	1	2015-11-12

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
LIDOCAINE	ACTIVE INGREDIENT	98PI200987	LIDOCAINE HYDROCHLORIDE (LIDOCAINE) GEL [GENSCO LABORATORIES, LLC]	1
LIDOCAINE	ACTIVE MOIETY	98PI200987	LIDOCAINE HYDROCHLORIDE (LIDOCAINE) GEL [GENSCO LABORATORIES, LLC]	1
FILIPENDULA ULMARIA FLOWER	INACTIVE INGREDIENT	06L18L32G6	LIDOCAINE HYDROCHLORIDE (LIDOCAINE) GEL [GENSCO LABORATORIES, LLC]	1
POLYETHYLENE GLYCOL 3350	INACTIVE INGREDIENT	G2M7P15E5P	LIDOCAINE HYDROCHLORIDE (LIDOCAINE) GEL [GENSCO LABORATORIES, LLC]	1
POLYETHYLENE GLYCOL 400	INACTIVE INGREDIENT	B697894SGQ	LIDOCAINE HYDROCHLORIDE (LIDOCAINE) GEL [GENSCO LABORATORIES, LLC]	1
QUERCUS ALBA WOOD	INACTIVE INGREDIENT	XR6BC2ZUAM	LIDOCAINE HYDROCHLORIDE (LIDOCAINE) GEL [GENSCO LABORATORIES, LLC]	1
WATER	INACTIVE INGREDIENT	059QF0KO0R	LIDOCAINE HYDROCHLORIDE (LIDOCAINE) GEL [GENSCO LABORATORIES, LLC]	1
ZINC ACETATE	INACTIVE INGREDIENT	FM5526K07A	LIDOCAINE HYDROCHLORIDE (LIDOCAINE) GEL [GENSCO LABORATORIES, LLC]	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 197 of 197 · 3,939 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Ultimate Topical Pain Relief Patch	CAPSAICIN AND MENTHOL, UNSPECIFIED FORM	Foshan Aqua Gel Biotech Co.,Ltd.	33c9f8ba-903e-249e-e054-00144ff8d46c	2017-11-06	Warnings	Exact identifier unii: L7T10EIP3A
Homeoplex D	GLYCERINUM, PHYTOLACCA DECANDRA, TARAXACUM OFFICINALE, ARSENICUM ALBUM, NITRICUM ACIDUM, NUX VOMICA, PETROLEUM, PHOSPHORICUM ACIDUM, PHOSPHORUS, ACETYLSALICYLICUM ACIDUM, GLONOINUM, INSULINUM (SUIS), LITHIUM CARBONICUM, THYROIDINUM (SUIS), SALICYLICUM ACIDUM, ADRENOCORTICOTROPHIN, CORTISONE ACETICUM, EUGENOL, STEARYL ALCOHOL, XYLITOL, FOLLICULINUM, BENZOICUM ACIDUM, CHLORINUM, POTASSIUM SORBATE, SORBITOL, RESORCINUM, BENZYL ALCOHOL, LACTICUM ACIDUM, ISOPROPYL PALMITATE, BORICUM ACIDUM, ACETICUM ACIDUM,	Supplement Clinic, LLC.	cd6b48ab-3566-484d-8deb-15ef6f8e7e8f	2017-11-01	Warnings	Exact identifier unii: PDC6A3C0OX
Sterile Water	WATER	Baxter Healthcare Corporation	ef3e79c5-3f58-4b36-a296-64b7d9a651c1	2017-10-17	Warnings, Adverse reactions	Exact identifier unii: 059QF0KO0R
Dollar General Medicated Pain Relief Patch	CAMPHOR, MENTHOL, METHYL SALICYLATE	DOLGENCORP, LLC	86b0bd7b-c31c-4c35-a5da-0deac9558abe	2017-10-01	Warnings	Exact identifier unii: L7T10EIP3A unii: LAV5U5022Y
Assured Vaporizing Chest Rub	CAMPHOR AND EUCALYPTUS OIL AND MENTHOL	Greenbrier International, Inc.	24fdad60-490d-6dc5-e054-00144ff8d46c	2017-08-31	Warnings	Exact identifier unii: L7T10EIP3A
Deeveeant Numb	LIDOCAINE	Valekista Limited	2d7b39cc-4f1b-4414-b129-88c56e159aba	2017-07-06	Warnings	Exact identifier unii: 98PI200987
MediNumb	LIDOCAINE	Valekista Limited	0e43648d-3dae-4faf-a6b4-d21c062e32e1	2017-07-06	Warnings	Exact identifier unii: 98PI200987
FIND BICHON CLEANSING MASK	GLYCERIN	Pioom Cosmetic Co.,ltd	50b7db48-7b55-6df4-e054-00144ff88e88	2017-05-30	Warnings	Exact identifier unii: PDC6A3C0OX
Eye Wash	WATER	CVS Pharmacy	049cee29-7ec2-4d5b-8308-f522acde43a7	2017-03-29	Warnings	Exact identifier unii: 059QF0KO0R
Studio 35 External Analgesic Medicated Body	MENTHOL AND ZINC OXIDE	Walgreen Co	2dd63063-45c1-4029-99ac-0962a27a5ddc	2017-02-08	Warnings	Exact identifier unii: L7T10EIP3A
CVS Sore Muscle Rub Vanishing Scent	MENTHOL	CVS Pharmacy	454bbde9-3076-6977-e054-00144ff88e88	2017-01-04	Warnings	Exact identifier unii: L7T10EIP3A
Professional Therapy MuscleCare Turbo	MENTHOL, CAMPHOR	Active and Innovative Inc.	42f1e14a-3ac6-01c1-e054-00144ff8d46c	2016-12-05	Warnings	Exact identifier unii: L7T10EIP3A
Dr. Blue	MENTHOL	Indiana Botanic Gardens	1b1150bd-e087-4d8f-b0d6-0d935cf6e31e	2016-11-01	Warnings	Exact identifier unii: L7T10EIP3A
Professional Therapy MuscleCare	CAMPHOR, MENTHOL	Active and Innovative Inc.	1ec95bbb-cd7d-2588-e054-00144ff8d46c	2016-08-11	Warnings	Exact identifier unii: L7T10EIP3A
Professional Therapy MuscleCare pain relieving gel Extra Strength	CAMPHOR, MENTHOL	Active and Innovative Inc.	1d2403d9-99c3-24f5-e054-00144ff8d46c	2016-08-10	Warnings	Exact identifier unii: L7T10EIP3A
MED AID CHEST RUB	MENTHOL AND CAMPHOR AND EUCALYPTUS OIL	Blue Cross Laboratories, Inc.	429041fe-55a5-4df1-b60d-721103e5c65e	2016-07-27	Warnings	Exact identifier unii: L7T10EIP3A
Sterile Water	WATER	Baxter Healthcare Company	210dc9ab-d6ca-4552-ac19-1be17792d290	2016-05-31	Warnings, Adverse reactions	Exact identifier unii: 059QF0KO0R
cf91f91e-c3d7-4710-9114-92ae656dd031			88dbd438-02c0-481a-bdb7-8b3f3c41fd46	2015-10-01	Warnings, Adverse reactions	Exact identifier spl id: cf91f91e-c3d7-4710-9114-92ae656dd031 spl set id: 88dbd438-02c0-481a-bdb7-8b3f3c41fd46
Eagle Brand Medicated Oil Aromatic	CAMPHOR, MENTHOL, METHYL SALICYLATE	Borden Company (Private) Limited	54e45d89-e8c3-6fc3-e063-6394a90aac4e	2015-06-15	Warnings	Exact identifier unii: L7T10EIP3A unii: LAV5U5022Y

Reported adverse events (FAERS/openFDA)#

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