NDC 51437-202 - Medicated Anti-Itch
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
- 51437-202
- Package NDCs from labels
- 51437-202-08
- Manufacturer
- Nootie, LLC
- Effective date
- 2016-08-16
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Medicated Anti-Itch - Nootie, LLC | Nootie, LLC | 2016-08-16 | OTC ANIMAL DRUG LABEL |
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 |
|---|---|---|---|---|---|---|
| DG Health Maximum Strength Pain Relieving Cleansing | BENZALKONIUM CL, LIDOCAINE HCL | Dollar General Corporation | 64f69315-77a3-49dc-940d-efd7a29c6645 | 2024-12-17 | Warnings | V13007Z41A |
| PRAX | PRAMOXINE HYDROCHLORIDE | Ferndale Laboratories, Inc. | 674f0d8b-3d50-42b1-8401-d2967bcdf5cf | 2024-12-17 | Warnings | 88AYB867L5 |
| DerMend Moisturizing Anti-Itch | PRAMOXINE HYDROCHLORIDE | Ferndale Laboratories, Inc. | 14c7fb1c-a310-4b12-ab2e-7f1c0801995c | 2024-12-17 | Warnings | 88AYB867L5 |
| Rite Aid Cala Itch Relief | PRAMOXINE HCL 1%, ZINC ACETATE 0.1% | Rite Aid | e29a9d59-4c7c-81aa-e053-2995a90a7056 | 2024-12-15 | Warnings | 88AYB867L5 |
| Good Sense Burn Relief Aloe | LIDOCAINE HCL | Geiss, Destin & Dunn, Inc | b5a7f629-a88d-b49d-e053-2995a90a49fa | 2024-12-15 | Warnings | V13007Z41A |
| QC Burn Relief Aloe | LIDOCAINE HCL | Chain Drug Marketing Association Inc | b5e76f0c-0bfe-b13e-e053-2995a90a0861 | 2024-12-15 | Warnings | V13007Z41A |
| Mentholatum Lidocaine Ice | LIDOCAINE HCL, MENTHOL | The Mentholatum Company | 4d74cbab-31cd-4579-9360-6852ee215b5e | 2024-12-13 | Warnings | V13007Z41A |
| VAGISIL Anti-Itch Medicated Wipes Maximum Strength | PRAMOXINE HYDROCHLORIDE | Combe Incorporated | b848f53d-8aea-4efe-aa2c-009d5121fc33 | 2024-12-12 | Warnings | 88AYB867L5 |
| Walgreens Cool n Heat | LIDOCAINE 4% | Walgreens | ce1b21d6-7aa6-2b18-e053-2995a90a4c91 | 2024-12-11 | Warnings | V13007Z41A |
| Pramoxine Itch relief | PRAMOXINE HCL 1% | CVS | e947694c-c122-0291-e053-2995a90ac39a | 2024-12-11 | Warnings | 88AYB867L5 |
| Serum X | LIDOCAINE HYDROCHLORIDE | AO Biologix, LLC | e07b6268-6400-6849-e053-2a95a90a8b3e | 2024-12-11 | Warnings | V13007Z41A |
| Blistex Ivarest Poison Ivy Itch | ZINC ACETATE AND PRAMOXINE HYDROCHLORIDE | Blistex Inc. | e1eaa3e7-12ab-4b7b-b1b0-77ab07b76a2a | 2024-12-11 | Warnings | 88AYB867L5 |
| Lidocaine Hydrochloride | LIDOCAINE HYDROCHLORIDE | McKesson Corporation dba SKY Packaging | 903cd7bd-6c3d-4068-bb24-e91b1ca1393d | 2024-12-10 | Warnings, Adverse reactions | V13007Z41A |
| Lidocaine 4 Percent | LIDOCAINE | SA3, LLC | 651710db-3c50-4bcf-b7cc-9ed24f663427 | 2024-12-09 | Warnings | V13007Z41A |
| AUVON Pain Relief Roll-on | LIDOCAINE | SHENZHEN YUWEN E-COMMERCE CO., LTD. | 8b30f623-6077-4f2e-8fa4-ce4a298953b5 | 2024-12-08 | Warnings | V13007Z41A |
| QC Medicated anti itch | PRAMOXINE HYDROCHLORIDE, MENTHOL | Chain Drug Marketing Association | b5e41e3a-81df-3a63-e053-2a95a90a5839 | 2024-12-08 | Warnings | 88AYB867L5 |
| QC Lidocaine Maximum Strength | LIDOCAINE HCL | Chain Drug Marketing Association | b5e1b1ab-8a95-2d2d-e053-2995a90aea53 | 2024-12-08 | Warnings | V13007Z41A |
| ITCH X | BENZYL ALCOHOL/PRAMOXINE HYDROCHLORIDE | BF ASCHER AND CO INC | 03c16d33-8f59-0184-e054-00144ff8d46c | 2024-12-05 | Warnings | 88AYB867L5 |
| PO First Aid Series BURN | LIDOCAINE HYDROCHLORIDE | Nantong Health & Beyond Hygienic Products Inc. | f1c349a8-216d-4233-922e-c95329a33d1e | 2024-12-05 | Warnings | V13007Z41A |
| Salonpas LIDOCAINE PLUS | BENZYL ALCOHOL, LIDOCAINE HYDROCHLORIDE | Hisamitsu America, Inc. | 364924d3-fac3-4f4e-9b40-decd4ec48245 | 2024-12-03 | Warnings | V13007Z41A |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.