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 173 of 197 · 3,939 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Eagle Brand Medicated Plaster	MENTHOL, METHYL SALICYLATE	Borden Company (Private) Limited	1026ba99-531a-c3be-e063-6294a90a0af4	2024-01-30	Warnings	Exact identifier unii: L7T10EIP3A unii: LAV5U5022Y
Joint and Muscle Pain	MENTHOL	Shaklee Corporation	3943824f-1f4f-4d6f-bd73-0b1be02162a5	2024-01-30	Warnings	Exact identifier unii: L7T10EIP3A
Mirakel Pain Relief Roll-On	LIDOCAINE HCL	Sanvio, Inc.	102f3618-13ad-37e3-e063-6294a90a8086	2024-01-30	Warnings	Exact identifier rxcui: 1010077
No More Products	GLYCERIN, KAOLIN, CALAMINE, MENTHOL	Sarati International, Inc	102e7dbb-06dc-f4d1-e063-6394a90aa3eb	2024-01-26	Warnings	Exact identifier unii: PDC6A3C0OX unii: L7T10EIP3A
Pranicura 5	GLYCERIN, KAOLIN, CALAMINE, MENTHOL	Sarati International, Inc.	0fe10710-ac59-4fc5-e063-6294a90a48fc	2024-01-26	Warnings	Exact identifier unii: PDC6A3C0OX unii: L7T10EIP3A
Blistex Lip Medex	PETROLATUM, MENTHOL, UNSPECIFIED FORM, CAMPHOR (SYNTHETIC), AND PHENOL	Blistex Inc.	8ad39005-9419-4f1a-a1ae-2f76d212455e	2024-01-26	Warnings	Exact identifier unii: L7T10EIP3A
Point Relief Cold Spot Pain Relieving	MENTHOL	Fabrication Enterprises	ad5d6f04-15e6-4548-95c2-32271c186bc1	2024-01-25	Warnings	Exact identifier unii: L7T10EIP3A
MIND BODY MATRIX PAIN RELIEF	MENTHOL	Functional Energetic, Inc.	3667dd0d-942e-4101-ba98-cb013ae77cf5	2024-01-25	Warnings	Exact identifier unii: L7T10EIP3A
Aspercreme	LIDOCAINE	Lead Chemical Co. Ltd.	275e1343-deef-424a-a883-5e780083af91	2024-01-25	Warnings	Exact identifier unii: 98PI200987
Lidocaine	LIDOCAINE	Bryant Ranch Prepack	65cf652c-87f2-43c6-a6f8-e4a83b42ce78	2024-01-24	Warnings, Adverse reactions	Exact identifier unii: 98PI200987
SUPER WHITE STUFF Pain Relief	MENTHOL	BLUE SPRING WELLNESS	e6d27df5-118c-4c6d-86e8-7b4401a39c76	2024-01-23	Warnings	Exact identifier unii: L7T10EIP3A
CHAPSTICK CLASSIC MEDICATED	CAMPHOR, MENTHOL, PETROLATUM	Haleon US Holdings LLC	b4259621-ff41-46cc-a658-b57bff3c1525	2024-01-23	Warnings	Exact identifier unii: L7T10EIP3A
Target Up and Up Pain Relief Menthol Topical Analgesic Roll-On	MENTHOL	TARGET CORPORATION	0f95fc55-8665-9e89-e063-6394a90a7891	2024-01-22	Warnings	Exact identifier unii: L7T10EIP3A
GENTEAL TEARS	DEXTRAN 70, GLYCERIN, HYPROMELLOSE	A-S Medication Solutions	a2b715e9-332d-4f0b-b8e5-ebc000681586	2024-01-21	Warnings	Exact identifier unii: PDC6A3C0OX
Sugar Free Cough Drops Honey Lemon	MENTHOL	Cardinal Health 110, Inc.	fe90dc33-2815-8296-e053-6294a90ac1df	2024-01-19	Warnings	Exact identifier unii: L7T10EIP3A
Sugar Free Cough Drops	MENTHOL	Cardinal Health 110, Inc.	fe91543e-a798-6399-e053-6394a90af5e5	2024-01-19	Warnings	Exact identifier unii: L7T10EIP3A
Sugar Free Cough Drops Black Cherry	MENTHOL	Cardinal Health 110, Inc.	fe90cf63-d286-fa5e-e053-6394a90a7759	2024-01-19	Warnings	Exact identifier unii: L7T10EIP3A
Cough Drops Menthol Honey Lemon	COUGH DROPS MENTHOL	Cardinal Health 110, Inc.	fe5b3f6d-2a2d-f322-e053-6394a90aba04	2024-01-19	Warnings	Exact identifier unii: L7T10EIP3A
Cough Drops Menthol	MENTHOL COUGH DROPS	Cardinal Health 110, Inc.	fe5b557e-a689-a32c-e053-6294a90aadbd	2024-01-19	Warnings	Exact identifier unii: L7T10EIP3A
Cough Drops Cherry	CHERRY FLAVOR COUGH DROPS	Cardinal Health 110, Inc.	fe5b5e57-1368-c62b-e053-6294a90ae82c	2024-01-19	Warnings	Exact identifier unii: L7T10EIP3A

Reported adverse events (FAERS/openFDA)#

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