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 82 of 201 · 4,013 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
SF Menthol Cough Drop	MENTHOL	HEB	3a443179-b7a6-3242-e054-00144ff8d46c	2025-12-13	Warnings	Exact identifier unii: L7T10EIP3A
Cherry cough drop	MENTHOL	HEB	39bd0ca1-348f-0ce1-e054-00144ff88e88	2025-12-13	Warnings	Exact identifier unii: L7T10EIP3A
Strawberry Cough Drops	MENTHOL	HEB	766236e2-3302-2232-e053-2991aa0af503	2025-12-13	Warnings	Exact identifier unii: L7T10EIP3A
Honey Lemon Cough Drop	MENTHOL	HEB	3a30a427-6ab4-24ae-e054-00144ff88e88	2025-12-13	Warnings	Exact identifier unii: L7T10EIP3A
HEB Menthol Cough Drops	MENTHOL	HEB	c197855d-15b4-38fc-e053-2a95a90a2dc7	2025-12-13	Warnings	Exact identifier unii: L7T10EIP3A
HEB SF Honey Lemon Cough Drops	MENTHOL	HEB	d09ed4bb-7595-5e54-e053-2a95a90aa109	2025-12-13	Warnings	Exact identifier unii: L7T10EIP3A
HEB Cherry Cough Drops	MENTHOL	HEB	c198e3c7-5ba7-ece6-e053-2995a90adb38	2025-12-13	Warnings	Exact identifier unii: L7T10EIP3A
HEB Honey Lemon Cough Drops	MENTHOL	HEB	c19a79bc-9872-2e87-e053-2a95a90a9427	2025-12-13	Warnings	Exact identifier unii: L7T10EIP3A
Vapor Rub	COUGH SUPPRESSANT	Neilmed Pharmaceuticals Inc.	39190f9f-8a5a-e4d8-e063-6294a90a57dd	2025-12-12	Warnings	Exact identifier unii: L7T10EIP3A
Joint and Muscle Relief	MENTHOL	Smart Cookie Solutions Inc.	45c24d56-4dc9-2884-e063-6294a90a52cc	2025-12-12	Warnings	Exact identifier unii: L7T10EIP3A
Orajel 4X Medicated For Toothache and Gum	BENZALKONIUM CHLORIDE, BENZOCAINE, MENTHOL, ZINC CHLORIDE	Church & Dwight Co., Inc.	999851ac-925c-7d1f-e053-2a95a90a240b	2025-12-12	Warnings	Exact identifier unii: L7T10EIP3A
Orajel 3X Medicated For Toothache and Gum	BENZOCAINE, MENTHOL, ZINC CHLORIDE	Church & Dwight Co., Inc.	99a2b061-0875-59a4-e053-2995a90ab373	2025-12-12	Warnings	Exact identifier unii: L7T10EIP3A
Orajel Antiseptic Rinse For All Mouth Sores	HYDROGEN PEROXIDE AND MENTHOL	Church & Dwight Co., Inc.	06188d36-0d60-6ae6-e054-00144ff8d46c	2025-12-12	Warnings	Exact identifier unii: L7T10EIP3A
Orajel 3X Medicated For All Mouth Sores	BENZOCAINE, MENTHOL, ZINC CHLORIDE	Church & Dwight Co., Inc.	99b589ac-9833-fb60-e053-2995a90a0935	2025-12-12	Warnings	Exact identifier unii: L7T10EIP3A
Orajel 4X Medicated For Toothache and Gum, Cream	BENZALKONIUM CHLORIDE, BENZOCAINE, MENTHOL, ZINC CHLORIDE	Church & Dwight Co., Inc.	999aa7b9-bf9e-9285-e053-2a95a90a345b	2025-12-12	Warnings	Exact identifier unii: L7T10EIP3A
Orajel 4X Medicated PM For Toothache and Gum	BENZALKONIUM CHLORIDE, BENZOCAINE, MENTHOL, ZINC CHLORIDE	Church & Dwight Co., Inc.	999cff2b-c23e-5abe-e053-2a95a90a7569	2025-12-12	Warnings	Exact identifier unii: L7T10EIP3A
Medicated Chest Rub	CAMPHOR, EUCALYPTUS OIL, MENTHOL	Cardinal Health, 110 dba LEADER	b7393668-1450-4e85-9793-d400daf39b43	2025-12-12	Warnings	Exact identifier unii: L7T10EIP3A
Careland Pain Relief Plus	CAMPHOR, MENTHOL, METHYL SALICYLATE	Planet (Anhui) Pharmaceutical Co., Ltd.	d9e63ddd-d003-45fa-b156-7f4452c28cbd	2025-12-12	Warnings	Exact identifier unii: L7T10EIP3A unii: LAV5U5022Y
Menthol cough drops	MENTHOL	Family Dollar	44bb3b95-b2ba-470e-e054-00144ff88e88	2025-12-12	Warnings	Exact identifier unii: L7T10EIP3A
menthol cough drops	MENTHOL	Family Dollar	44bb9c7b-994b-4ab8-e054-00144ff8d46c	2025-12-12	Warnings	Exact identifier unii: L7T10EIP3A

Reported adverse events (FAERS/openFDA)#

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