NDC 59050-059 - Sting Relief Pad
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
- 59050-059
- Manufacturer
- Acme United Corporation
- Effective date
- 2024-11-19
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Sting Relief Pad - Acme United Corporation | Acme United Corporation | 2024-11-19 | HUMAN OTC 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 |
|---|---|---|---|---|---|---|
| Isopropyl Alcohol | ISOPROPYL ALCOHOL | JHK Inc | abae6a80-e859-47b5-8e34-d391eb854583 | 2024-04-26 | Warnings | ND2M416302 |
| HYDROCORTISONE | HYDROCORTISONE ACETATE | JHK Inc dba American Safety & First Aid | 64adc8d0-7ca4-4c1a-813f-f1df47e916f2 | 2024-04-25 | Warnings | M017 |
| HealthWise Lidocaine Plus Cream | BENZYL ALCOHOL, LIDOCAINE HYDROCHLORIDE | Veridian Healthcare | 16f26249-b508-2c6e-e063-6394a90a265b | 2024-04-25 | Warnings | M017 |
| Hydrocortisone Cream with Aloe | HYDROCORTISONE | Cardinal Health 110 dba LEADER | 16f2f3cb-4611-5867-e063-6394a90af107 | 2024-04-25 | Warnings | M017 |
| Burn | LIDOCAINE HYDROCHLORIDE | JHK Inc | 5a4ac4cc-015a-48e7-81f8-93a895049afd | 2024-04-25 | Warnings | M017 |
| Antiseptic | BENZALKONIUM CHLORIDE, BENZOCAINE | JHK Inc | 0ac5d890-c262-4a30-9fd8-2de6cb0f7601 | 2024-04-25 | Warnings | U3RSY48JW5 |
| PEMF Optimizer | AQUA SULIS, ARGENTUM METALLICUM, AURUM METALLICUM, CUPRUM METALLICUM, LAPIS ALBUS, MANGANUM METALLICUM VANADIUM METALLICUM VISCUM ALBUM, ZINCUM METALLICUM | Deseret Biologicals, Inc. | 97d57469-4c5b-4d3f-9398-3a1a6617a649 | 2024-04-23 | Warnings | 059QF0KO0R |
| Cold Therapy Pain Relief | MENTHOL, UNSPECIFIED FORM | Walgreen Co. | ede15818-5d17-477d-a8be-7b36bb0770a6 | 2024-04-22 | Warnings | M017 |
| Anti Itch | HYDROCORTISONE | Neilmed Pharmaceuticals Inc. | 14b4f066-fde4-ac97-e063-6394a90ae64c | 2024-04-20 | Warnings | M017 |
| Walgreens Cold Therapy Pain Relief Patch | MENTHOL 5% | Walgreens Company | e33c90d1-2729-970f-e053-2995a90ad97a | 2024-04-18 | Warnings | M017 |
| HealthWise Cold Therapy Pain Relief Patch | MENTHOL | Veridian Healthcare | 0ce356e0-90a3-ad52-e063-6294a90a404a | 2024-04-18 | Warnings | M017 |
| Walgreens Scalp Relief External analgesic | HYDROCORTISONE | Walgreen Company | da0a24c7-9295-4f22-b2c7-40000dad4b81 | 2024-04-18 | Warnings | M017 |
| HealthWise 3x Medicated Pain Relief Patch | CAMPHOR,MENTHOL, METHYL SALICYLATE | Veridian Healthcare | 164d4d62-00c0-e06d-e063-6294a90abd73 | 2024-04-17 | Warnings | M017 |
| TIGER Balm PAIN RELIEVING HYDROGEL | CAMPHOR (SYNTHETIC), LEVOMENTHOL, AND CAPSICUM | Haw Par Healthcare Ltd. | ca601b02-e9be-4d8d-a384-c62553302ceb | 2024-04-16 | Warnings | M017 |
| Quality Choice Oral Pain Relief | BENZOCAINE 20%, BENZALKONIUM CHLORIDE 1% | Quality Choice (CHAIN DRUG MARKETING ASSOCIATION) | 162702b4-4bf7-8868-e063-6294a90a5921 | 2024-04-15 | Warnings | U3RSY48JW5 |
| Gelato Topical Anesthetic | BENZOCAINE | Mycone Dental Supply Co., Inc DBA Keystone Industries and Deepak Products Inc | 9991de96-99a1-42f0-9ddd-e530ca9ceab1 | 2024-04-11 | Warnings | U3RSY48JW5 |
| Sterile Water | WATER | Hikma Pharmaceuticals USA Inc. | 78ef7ad3-451d-43d0-a9b6-5cf0aadca003 | 2024-04-10 | Warnings, Adverse reactions | 059QF0KO0R |
| Sterile Water | WATER | B. Braun Medical Inc. | 8fc8d87a-3951-4ac5-97df-c161ffc90475 | 2024-04-10 | Warnings, Adverse reactions | 059QF0KO0R |
| Lidocaine Pain Relief Patch | LIDOCAINE PAIN RELIEF PATCH | Henan Enokon Medical Instrument Co., Ltd. | 1592a40a-a647-34bd-e063-6394a90a0a10 | 2024-04-08 | Warnings | M017 |
| Menticam | CAMPHOR, MENTHOL, METHYL SALICYLATE | PureTek Corporation | 081837a8-9669-be1f-e063-6394a90a9d20 | 2024-04-05 | Warnings | M017 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.