Sunflower
Helianthus annuus · Solution · Intradermal, Percutaneous, Subcutaneous
No FDA structured label text is available for Sunflower. The NDC listings below come from the FDA National Drug Code directory.
Active ingredients
- Helianthus Annuus Pollen in 5 products
Sunflower NDC products (5)
| NDC | Strength & form | Labeler | Type |
|---|---|---|---|
| 22840-1503 | Helianthus Annuus Pollen .1 g/mL Solution | Greer Laboratories, Inc. | BLA |
| 22840-1504 | Helianthus Annuus Pollen 40000 [PNU]/mL Solution | Greer Laboratories, Inc. | BLA |
| 22840-1505 | Helianthus Annuus Pollen 1000 [PNU]/mL Solution | Greer Laboratories, Inc. | BLA |
| 22840-1506 | Helianthus Annuus Pollen .001 g/mL Solution | Greer Laboratories, Inc. | BLA |
| 22840-5502 | Helianthus Annuus Pollen .05 g/mL Solution | Greer Laboratories, Inc. | BLA |
Frequently asked questions
Who makes Sunflower?
Sunflower is listed by 1 labeler in the FDA NDC directory, including Greer Laboratories, Inc..