Nettle
Urtica dioica · Solution · Subcutaneous, Intradermal, Percutaneous
No FDA structured label text is available for Nettle. The NDC listings below come from the FDA National Drug Code directory.
Active ingredients
- Urtica Dioica Pollen in 5 products
Nettle NDC products (5)
| NDC | Strength & form | Labeler | Type |
|---|---|---|---|
| 0268-7110 | Urtica Dioica Pollen .05 g/mL Injection, Solution | ALK-Abello, Inc. | BLA |
| 22840-1356 | Urtica Dioica Pollen .05 g/mL Solution | Greer Laboratories, Inc. | BLA |
| 22840-1357 | Urtica Dioica Pollen 20000 [PNU]/mL Solution | Greer Laboratories, Inc. | BLA |
| 22840-1358 | Urtica Dioica Pollen .001 g/mL Solution | Greer Laboratories, Inc. | BLA |
| 22840-5317 | Urtica Dioica Pollen .025 g/mL Solution | Greer Laboratories, Inc. | BLA |
Frequently asked questions
Who makes Nettle?
Nettle is listed by 2 labelers in the FDA NDC directory, including ALK-Abello, Inc., Greer Laboratories, Inc..