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 148 of 199 · 3,977 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Mentholatum Deep Heating Rub Extra Strength	MENTHOL, METHYL SALICYLATE	The Mentholatum Company	f5684158-0d83-4031-b493-5422ddc73e78	2024-12-13	Warnings	Exact identifier unii: L7T10EIP3A unii: LAV5U5022Y
Mentholatum Lavender Vaporizing Rub	CAMPHOR, EUCALYPTUS OIL, MENTHOL	The Mentholatum Company	6f208c05-617d-492a-a016-e9d6be3c971f	2024-12-13	Warnings	Exact identifier unii: L7T10EIP3A
Discount Drug Mart Anti-Itch	CAMPHOR, MENTHOL	Discount Drug Mart	87d379da-103a-c751-e053-2995a90a56de	2024-12-13	Warnings	Exact identifier unii: L7T10EIP3A
Salonpas Arthritis Pain	MENTHOL, METHYL SALICYLATE	Hisamitsu Pharmaceutical Co., Inc.	a6518167-fe32-43b2-b736-ba01ac69c12d	2024-12-13	Warnings	Exact identifier unii: L7T10EIP3A unii: LAV5U5022Y
HealthWise Medicated Foot Powder	MENTHOL	Veridian Healthcare	2916a0c3-2d66-d079-e063-6394a90acd6b	2024-12-12	Warnings	Exact identifier unii: L7T10EIP3A
Ease Your Pain	MENTHOL	Proximity Capital Partners LLC dba Asutra	83366ae1-e1d9-2a30-e053-2a91aa0a1cc4	2024-12-12	Warnings	Exact identifier unii: L7T10EIP3A
Natural Seal Itch Relief for Kids	LIDOCAINE	Kericure Inc.	31cc0c95-5864-4737-b085-8f58e00f4f05	2024-12-12	Warnings	Exact identifier unii: 98PI200987
Walgreens Cool and Heat	MENTHOL 16%	Walgreens	ce1585f4-ca65-8d0c-e053-2995a90a8e89	2024-12-11	Warnings	Exact identifier unii: L7T10EIP3A
Walgreens Cool n Heat	LIDOCAINE 4%	Walgreens	ce1b21d6-7aa6-2b18-e053-2995a90a4c91	2024-12-11	Warnings	Exact identifier unii: L7T10EIP3A
Walgreens Pain Burn Itch Relief	BENZOCAINE 20%, MENTHOL 0.5%	Walgreens	cc6e4b42-fdd8-6ff7-e053-2995a90a3d1d	2024-12-11	Warnings	Exact identifier unii: L7T10EIP3A
CVS Pain Relief	MENTHOL 4%	CVS	d1660d55-1ee0-7aa2-e053-2995a90a6579	2024-12-11	Warnings	Exact identifier unii: L7T10EIP3A
CVS Muscle Rub	MENTHOL 10%, METHYL SALICYLATE 15%	CVS Health	c72c9a95-4226-6d69-e053-2a95a90a8e1c	2024-12-11	Warnings	Exact identifier unii: L7T10EIP3A unii: LAV5U5022Y
BENGAY ULTRA STRENGTH NON-GREASY	CAMPHOR (SYNTHETIC), MENTHOL, UNSPECIFIED FORM, AND METHYL SALICYLATE	Kenvue Brands LLC	0a41ec65-bd0b-4fc6-807d-74f353341cc7	2024-12-11	Warnings	Exact identifier unii: L7T10EIP3A unii: LAV5U5022Y
PlusCBD Pain Cream (Penetrating) 2oz	CAMPHOR, MENTHOL	CV Sciences, Inc.	ca39d327-6bf3-3408-e053-2a95a90af2d5	2024-12-11	Warnings	Exact identifier unii: L7T10EIP3A
Blistex Medicated	DIMETHICONE, CAMPHOR (SYNTHETIC), MENTHOL, AND PHENOL	Blistex Inc.	e95439d3-f12b-4c1c-999a-79f2ddba4cfb	2024-12-11	Warnings	Exact identifier unii: L7T10EIP3A
Blistex Ivarest Poison Ivy Itch	ZINC ACETATE AND PRAMOXINE HYDROCHLORIDE	Blistex Inc.	e1eaa3e7-12ab-4b7b-b1b0-77ab07b76a2a	2024-12-11	Warnings	Exact identifier unii: FM5526K07A
Fendall Pure Flow	PURIFIED WATER	Honeywell Safety Products USA, Inc.	afda6fc3-7615-b0be-e053-2995a90a6208	2024-12-10	Warnings	Exact identifier unii: 059QF0KO0R
TheraCare Maximum Strength Pain Relief Patch	LIDOCAINE	Veridian Healthcare	dfaf8a77-2276-4791-e053-2a95a90a3288	2024-12-10	Warnings	Exact identifier unii: 98PI200987
NATURAL LEMON MINT HERB THROAT DROPS	MENTHOL	Ricola USA Inc.	763e8234-60be-4b1f-9f78-01c574f35d0a	2024-12-10	Warnings	Exact identifier unii: L7T10EIP3A
DUAL ACTION CHERRY COUGH SUPPRESSANT ORAL ANESTHETIC	MENTHOL	Ricola USA Inc.	09141018-37ba-4c93-9051-1ed129c448c1	2024-12-10	Warnings	Exact identifier unii: L7T10EIP3A

Reported adverse events (FAERS/openFDA)#

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