NDC 69571-002-01 - Assured
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
- 69571-002
- Requested NDC
- 69571-002-01
- Package NDCs from labels
- 69571-002-01, 69571-002-02
- Manufacturer
- Anhui NHU Pharmaceutical Co., Ltd.
- Effective date
- 2015-12-27
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Drug Facts | Anhui NHU Pharmaceutical Co., Ltd. | 2015-12-27 | 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 |
|---|---|---|---|---|---|---|
| YULAM DIE DA WAN HUA PAIN RELIEVING | MENTHOL AND CAMPHOR | MADISON ONE ACME INC | 1ba3c31b-2737-4b55-a0ea-90013a1d8cf4 | 2025-11-12 | Warnings, Adverse reactions | L7T10EIP3A |
| TattooNumb | LIDOCAINE HYDROCHLORIDE | Sambria Pharmaceuticals, LLC | d9c4d664-54de-40c2-8836-72b60e6d9ac0 | 2025-11-12 | Warnings | V13007Z41A |
| BeardedMoney | LIDOCAINE HYDROCHLORIDE | Sambria Pharmaceuticals, LLC | 35ff688b-75c5-4780-b294-192af780d705 | 2025-11-12 | Warnings | V13007Z41A |
| NeuroMed 7 Topical Pain Relief | LIDOCAINE HYDROCHLORIDE | Sambria Pharmaceuticals, LLC | f199f56b-d971-4cf8-834d-babb5c2ff81a | 2025-11-12 | Warnings | V13007Z41A |
| NeuroMed Topical Anesthetic 7 | LIDOCAINE HYDROCHLORIDE | Sambria Pharmaceuticals | 8a2b6b76-6bcc-4f52-b037-e6cbc74f8377 | 2025-11-12 | Warnings | V13007Z41A |
| NeuroMed Topical Anesthetic 7 | LIDOCAINE HYDROCHLORIDE | Sambria Pharmaceuticals | 67b25c37-db32-4980-88b0-b07712345939 | 2025-11-12 | Warnings | V13007Z41A |
| ZHENG GU SHUI | CAMPHOR, MENTHOL | GUANGXI YULIN PHARMACEUTICAL GROUP CO LTD | 17552943-4f11-42d6-ad41-fbc53f2bbd9a | 2025-11-12 | Warnings, Adverse reactions | L7T10EIP3A |
| Hempvana Cold As Ice Pain Relief | MENTHOL | Telebrands Corp | 95e84bb9-ba2e-5009-e053-2995a90a4362 | 2025-11-12 | Warnings | L7T10EIP3A |
| Lidozall | LIDOCAINE HYDROCHLORIDE | V2 Pharma LLC | 1eb2dfb2-3ad1-488b-aed9-17220e34a10c | 2025-11-12 | Warnings | V13007Z41A |
| Lidozall Plus | LIDOCAINE HYDROCHLORIDE | V2 Pharma LLC | ba3cbb15-f4ed-443e-af43-a758481acb0b | 2025-11-12 | Warnings | V13007Z41A |
| Eyesaline Eyewash Concentrate | PURIFIED WATER | Honeywell Safety Products USA, Inc. | 3765c251-eb14-d60f-e063-6294a90a6a4d | 2025-11-12 | Warnings | 059QF0KO0R |
| Eyesaline Emergency Eyewash | PURIFIED WATER | Honeywell Safety Products USA, Inc. | 37f244fd-c02f-e66a-e063-6394a90aed81 | 2025-11-12 | Warnings | 059QF0KO0R |
| Rapid Relief | COLD RELIEF PATCH 5% MENTHOL | RAPID AID VIET NAM COMPANY LIMITED | 434c13c2-52ee-000f-e063-6294a90af7e7 | 2025-11-11 | Warnings | L7T10EIP3A |
| Rapid Relief | PAIN RELIEF PATCH LIDOCAINE 4% MENTHOL 1% | RAPID AID VIET NAM COMPANY LIMITED | 434df0be-49ff-aa56-e063-6394a90a3b5a | 2025-11-11 | Warnings | L7T10EIP3A |
| TopCare Pain Relief Maximum Strength | LIDOCAINE HYDROCHLORIDE | TOPCO ASSOCIATES | b0ae3a7c-52d1-4923-bd50-6bb3749006c8 | 2025-11-11 | Warnings | V13007Z41A |
| SunDrops 77 | BENZALKONIUM CHLORIDE | Sunburst Chemicals, Inc. | fc0ba65c-5307-4251-a60b-cde84ad56ad8 | 2025-11-11 | Warnings | F5UM2KM3W7 |
| SunDrops 87 | BENZALKONIUM CHLORIDE | Sunburst Chemicals, Inc. | 584ea129-aaf2-402f-b9f1-3fec2a23a21c | 2025-11-11 | Warnings | F5UM2KM3W7 |
| Comfortcaine | LIDOCAINE HCL | QS Key West Aloe, LLC | 831b7c11-e437-4e74-808e-c9c1eb8b82f6 | 2025-11-11 | Warnings | V13007Z41A |
| DermaNumb Analgesic | LIDOCAINE HCL | A.T.S. Laboratories, LLC | 0ea46890-45c3-4732-bc47-227f7c67daf1 | 2025-11-11 | Warnings | V13007Z41A |
| Derma Numb Pain Relief | LIDOCAINE HCL | A.T.S. Laboratories, LLC | 710991ae-8f82-4893-93a7-0ef3f815d132 | 2025-11-11 | Warnings | V13007Z41A |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.