PMDA drug package insert
ルルのど飴DXG
PMDA OTC drug · 第一三共ヘルスケア（株） · package insert Jun 18, 2021
Key facts
| Brand names | ルルのど飴DXG |
|---|---|
| Companies | 製造販売元／（株）浅田飴,販売会社／第一三共ヘルスケア（株） |
| Product type | OTC drug |
| OTC risk class | なし |
| OTC dosage form | その他 |
| OTC effect category | その他（いずれの薬効群にも属さない製剤） |
| Package insert date | Jun 18, 2021 |
| PMDA document key | 710070_J1001000377 |
| PMDA company code | 710070 |
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: