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 169 of 198 · 3,957 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Sterile Water	WATER	Becton Dickinson and Company	6e43c5a3-dad2-49ed-b500-964cb4563cc9	2024-05-31	Warnings, Adverse reactions	Exact identifier unii: 059QF0KO0R
Methyl Salicylate 25 Percent	METHYL SALICYLATE	Alexso, Inc	d8b8b0ba-69e9-4965-bf9b-6db21db69b34	2024-05-23	Warnings	Exact identifier unii: LAV5U5022Y
Meijer Medicated Chest Rub	CAMPHOR, MENTHOL, EUCALYPTUS OIL	Meijer Distribution	07ecc6a7-bbe3-35cf-e063-6394a90a2180	2024-05-22	Warnings	Exact identifier unii: L7T10EIP3A
TheraCare 4% Lidocaine and 1% Menthol Cream	MENTHOL AND LIDOCAINE	Veridian Healthcare	c80ba251-91a5-0858-e053-2995a90a9cff	2024-05-21	Warnings	Exact identifier unii: 98PI200987 unii: L7T10EIP3A
HealthWise Menthol Roll-On	MENTHOL	Veridian Healthcare	102d57a5-6449-f825-e063-6294a90a8844	2024-05-21	Warnings	Exact identifier unii: L7T10EIP3A
careone clearlax	POLYETHYLENE GLYCOL 3350	Retail Business Services, LLC	2378b76d-dc5a-4ff1-ad48-9f3e0c31c6cd	2024-05-19	Warnings	Exact identifier unii: G2M7P15E5P
HealthWise Menthol 4% Roll-On	MENTHOL	Veridian Healthcare	1894ef00-ba05-0e02-e063-6394a90ab982	2024-05-16	Warnings	Exact identifier unii: L7T10EIP3A
Menthol Cough Drops	MENTHOL	Target Corporation Inc.	187622dc-ecde-181d-e063-6294a90a4e8f	2024-05-14	Warnings	Exact identifier unii: L7T10EIP3A
Lemon Mint Drops	MENTHOL	Target Corporation Inc.	1876df19-398a-23d8-e063-6394a90ae7e8	2024-05-14	Warnings	Exact identifier unii: L7T10EIP3A
Extra Strength Itch Stopping	ITCH STOPPING CREAM	Universal Distribution Centre LLC	b9a42aa3-1903-76f0-e053-2a95a90a51d1	2024-05-13	Warnings	Exact identifier unii: FM5526K07A
Calamine Clear	PRAMOXINE HYDROCHLORIDE AND ZINC ACETATE LOTION	Cardinal Health, 110 dba Leader	7f733c0a-82b2-d3b0-e053-2991aa0a6b0f	2024-05-13	Warnings	Exact identifier unii: FM5526K07A
Eagle Brand Medicated Oil Aromatic	CAMPHOR, MENTHOL, METHYL SALICYLATE	Borden Company (Private) Limited	0e808f89-62dc-3790-e063-6394a90a2351	2024-05-13	Warnings	Exact identifier unii: L7T10EIP3A unii: LAV5U5022Y
LIDOTHOL	LIDOCAINE AND MENTHOL	Advanced Rx Pharmacy of Tennessee, LLC	181f0806-dab7-410c-e063-6294a90ac09c	2024-05-10	Warnings, Adverse reactions	Exact identifier unii: 98PI200987 unii: L7T10EIP3A
Sodium Phenylacetate and Sodium Benzoate	SODIUM PHENYLACETATE AND SODIUM BENZOATE	FOSUN PHARMA USA INC	cee1e9a2-bbe5-2419-e053-2a95a90ac3ef	2024-05-09	Warnings, Adverse reactions	Exact identifier unii: OJ245FE5EU
Fleet	GLYCERIN	C.B. Fleet Company, Inc.	381f4179-0c3b-41f8-927c-c88534ebe06d	2024-05-06	Warnings	Exact identifier unii: PDC6A3C0OX
Professional Therapy MuscleCare Pro Pain Relieving Cold Gel	CAMPHOR, MENTHOL	ACTIVE AND INNOVATIVE, LLC	1794c512-5f42-4ec3-e063-6394a90a87cd	2024-05-03	Warnings	Exact identifier unii: L7T10EIP3A
Professional Therapy MuscleCare Pro	MENTHOL AND CAMPHOR	ACTIVE AND INNOVATIVE, LLC	17961a84-6bee-c75f-e063-6394a90af576	2024-05-03	Warnings	Exact identifier unii: L7T10EIP3A
HealthWise 3x Medicated Pain Relief Patch 120 Bulk	CAMPHOR,MENTHOL, METHYL SALICYLATE	Veridian Healthcare	17545078-05e1-9338-e063-6394a90a678c	2024-04-30	Warnings	Exact identifier unii: LAV5U5022Y
Professional Therapy MuscleCare Pro Roll-on	CAMPHOR, MENTHOL	ACTIVE AND INNOVATIVE, LLC	1755ec89-c404-1c17-e063-6394a90ab9fb	2024-04-30	Warnings	Exact identifier unii: L7T10EIP3A
PAIN RELIEF Gel-Roll On	MENTHOL	Shanghai Chuangshi Medical Technology (Group) Co., Ltd.	f0bc2a14-6bda-428c-e053-2995a90a4ced	2024-04-29	Warnings	Exact identifier unii: L7T10EIP3A

Reported adverse events (FAERS/openFDA)#

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