Allergy Relief
- Product NDC
- 59726-203
- 11-digit product format
- 597260203
- Labeler code
- 59726
- Product ID
- 59726-203_c180ed31-17af-48cf-a484-dc1e96911704
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- fluticasone propionate
- Dosage form
- SPRAY, METERED
- Route
- NASAL
- Labeler
- P & L Development, LLC
- Application
- ANDA208150
- Marketing category
- ANDA
- Marketing start
- 2026-05-15
- Substance
- FLUTICASONE PROPIONATE
- Active strength
- 50 ug/1
- Pharmacologic classes
- Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| O2GMZ0LF5W | FLUTICASONE PROPIONATE | 80474-14-2 | FLUTICASONE PROPIONATE |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 59726-203-38 | 59726020338 | 1 BOTTLE, SPRAY in 1 CARTON (59726-203-38) / 72 SPRAY, METERED in 1 BOTTLE, SPRAY | 2026-05-15 | No | No | Historical |
| 59726-203-54 | 59726020354 | 1 BOTTLE, SPRAY in 1 CARTON (59726-203-54) / 120 SPRAY, METERED in 1 BOTTLE, SPRAY | 2026-05-15 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Drug Facts | P & L Development, LLC | 2026-05-26 | HUMAN OTC DRUG LABEL | 3 |