PMDA drug package insert
オノフェ乳状液20
PMDA OTC drug · マイクロウェーバー（株） · package insert Jan 7, 2016
Key facts
| Brand names | オノフェ乳状液20 |
|---|---|
| Companies | 製造販売元／万協製薬（株）,販売元／マイクロウェーバー（株） |
| Product type | OTC drug |
| OTC risk class | 第３類医薬品 |
| OTC dosage form | 液剤 |
| OTC effect category | 皮膚軟化薬（吸出しを含む） |
| Package insert date | Jan 7, 2016 |
| PMDA document key | 630357_J1501000287 |
| PMDA company code | 630357 |
At a glance
- 1–9 Package insert revisions
- None Related PMDA documents
- None Safety communications
- No PMDA review report published
- No Risk management plan (RMP)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About PMDA approved drugs and package inserts (Japan)
Japan's PMDA publishes the package insert (添付文書) of every prescription drug, OTC drug and regenerative medical product, with brand and nonproprietary names, YJ codes and approval numbers. Names appear in Japanese as published.
Source: Pharmaceuticals and Medical Devices Agency (PMDA), Japan, package insert database · Source date: