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 | 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 | 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 | 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 | 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 | 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 | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| 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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Sunmark Lubricant Eye Drops | POLYPROPYLENE GLYCOL 400, PROPYLENE GLYCOL | Strategic Sourcing Services LLC | b117ff0a-1a48-4022-96e6-52bc45f056fc | 2023-12-23 | Warnings | B697894SGQ |
| Sunmark Dry Eye Relief | GLYCERIN, HYPROMELLOSE, POLYETHYLENE GLYCOL 400 | Strategic Sourcing Services LLC | 043ccc34-44ee-416a-88bc-f247774e9075 | 2023-12-23 | Warnings | B697894SGQ PDC6A3C0OX |
| Sunmark Lubricating Tears | POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL | Strategic Sourcing Services LLC | 58f0b6d7-6072-40fd-ba72-b3ed68834791 | 2023-12-23 | Warnings | B697894SGQ |
| Leader Eye Wash | PURIFIED WATER | Cardinal Health | 8d3ad11f-1945-f838-e053-2995a90a7aa5 | 2023-12-23 | Warnings | 059QF0KO0R |
| Rite Aid Eye Drops Dry Eye Relief | GLYCERIN, HYPROMELLOSE, POLYETHYLENE GLYCOL 400 | Rite Aid Corporation | fa1b5b66-9643-e9a7-e053-6394a90ae3cf | 2023-12-23 | Warnings | B697894SGQ PDC6A3C0OX |
| Signature Care Lubricant Eye Drops Long Lasting | POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL | Better Living Brands, LLC | 05a63929-fccd-2936-e063-6294a90aeac5 | 2023-12-23 | Warnings | B697894SGQ |
| Meijer Lubricant Eye Drops | POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL | Meijer Distribution, Inc. | 9feadde4-fbe5-0c9e-e053-2995a90a9b30 | 2023-12-22 | Warnings | B697894SGQ |
| Meijer Maximum Redness Relief and Lubricant | GLYCERIN, NAPHAZOLINE HCI | Meijer Distribution, Inc. | 9feb1818-c79b-23bf-e053-2995a90a1084 | 2023-12-22 | Warnings | PDC6A3C0OX |
| Meijer Redness Relief | GLYCERIN, NAPHAZOLINE HCI | Meijer Distribution, Inc. | 9fea4e43-7525-bb66-e053-2a95a90acee9 | 2023-12-22 | Warnings | PDC6A3C0OX |
| Meijer Ultra Lubricant Eye Drops High Performance | POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL | Meijer Distribution, Inc. | a0846e3e-687c-fd55-e053-2995a90a673e | 2023-12-22 | Warnings | B697894SGQ |
| Meijer Advanced Redness and Irritation Relief | DEXTRAN 70, POLYETHYLENE GLYCOL 400, POVIDONE, TETRAHYDROZOLINE HCI | Meijer Distribution, Inc. | 9fea6d7a-a2cd-d26e-e053-2995a90a15f8 | 2023-12-22 | Warnings | B697894SGQ |
| Meijer Dry Eye Relief | GLYCERIN, HYPROMELLOSE, POLYETHYLENE GLYCOL 400 | Meijer Distribution, Inc. | 9feaa5e2-6aca-96e8-e053-2a95a90a54bd | 2023-12-22 | Warnings | B697894SGQ PDC6A3C0OX |
| Dermoplast Pain relieving | BENZOCAINE, MENTHOL | Advantice Health | dad00c95-4e11-3eec-e053-2a95a90a7a18 | 2023-12-21 | Warnings | L7T10EIP3A |
| HempNesic | MENTHOL, CAMPHOR | Blaine Labs Inc. | 0239ada0-644d-4ef4-a3b8-df70246a3bc2 | 2023-12-21 | Warnings | L7T10EIP3A |
| HempNesic | MENTHOL, CAMPHOR | Blaine Labs Inc. | a698502d-c1c5-41ca-8142-74338b834c8b | 2023-12-21 | Warnings | L7T10EIP3A |
| Valtrum IMMEDIATE ACTION TOPICAL ANALGESIC | CAMPHOR, MENTHOL, METHYL SALICYLATE | LABORATORIOS QUANTIUM LLC | c4efa317-8dd1-49e1-b7ca-9df2147edd3e | 2023-12-21 | Warnings | L7T10EIP3A LAV5U5022Y |
| NUMSTAT Antiseptic and Pain Relieving Prep Pad | ALCOHOL, MENTHOL, AND BENZOCAINE PREP PAD | Spectra Medical Devices, LLC | 07d20040-9dd9-0aba-e063-6294a90ab7cf | 2023-12-20 | Warnings | L7T10EIP3A |
| CVS Cold and Hot Roll-On | COOL AND HEAT PAIN RELIEF | CVS Pharmacy | b8cc578a-be6d-90c0-e053-2995a90a7742 | 2023-12-20 | Warnings | L7T10EIP3A |
| CVS Itch Relief | PRAMOXINE HYDROCHLORIDE AND ZINC ACETATE | CVS Pharmacy | c60cfbf2-6788-43dc-b23a-e3433b7f3265 | 2023-12-20 | Warnings | FM5526K07A |
| Walgreens Multi-Symptom Relief Eye Drops | GLYCERIN, HYPROMELLOSE, POLYETHYLENE GLYCOL 400, TETRAHYDROZOLINE HCL, ZINC SULFATE | Walgreen Co. | a03789ce-66bd-7b12-e053-2995a90af85a | 2023-12-20 | Warnings | B697894SGQ PDC6A3C0OX |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.