Indications and uses
Temporarily relieves these symptoms of hay fever or other upper respiratory allergies: • nasal congestion • itchy nose • runny nose • itchy, watery eyes • sneezing
Temporarily relieves these symptoms of hay fever or other upper respiratory allergies: • nasal congestion • itchy nose • runny nose • itchy, watery eyes • sneezing
• read the Quick Start Guide for how to: o prime the bottle o use the spray o clean the spray nozzle • shake gently before each use • use this product only once a day • do not use more than directed ADULTS AND CHILDREN 12 YEARS OF AGE AND OLDER • Week 1- use 2 sprays in each nostril once daily • Week 2 through 6 months- use 1 or 2 sprays in each nostril once daily, as needed to treat your symptoms • After 6 months...
• you may start to feel relief the first day and full effect after several days of regular, once-a-day use • store between 4° and 30°C (39° and 86°F) • keep this label and enclosed materials. They contain important additional information.
Fluticasone propionate (glucocorticoid)* 50 mcg
*read the Question & Answer Leaflet
Allergy symptom reliever
Temporarily relieves these symptoms of hay fever or other upper respiratory allergies:
Only for use in the nose. Do not spray into your eyes or mouth.
have or had glaucoma or cataracts
ask a health professional before use.
In case of overdose, get medical help or contact a Poison Control Center right away at 1 (800) 222-1222.
ADULTS AND CHILDREN 12 YEARS OF AGE AND OLDER
CHILDREN 4 TO 11 YEARS OF AGE
CHILDREN UNDER 4 YEARS OF AGE
benzalkonium chloride, dextrose, microcrystalline cellulose, phenylethyl alcohol, polysorbate 80, sodium carboxymethylcellulose, water for injection
Call 833-358-6431 Monday to Friday 9:00am to 7:00pm EST
Fluticasone Propionate Nasal Spray Allergy Relief helps relieve a broad range of uncomfortable symptoms like congestion and itchy eyes.
These symptoms can be triggered by allergens like pollen, mold, dust or pet dander.
CAN HELP WITH:
Be sure to read the Quick Start Guide and Question & Answer Leaflet inside package.
TAMPER-EVIDENT features for your protection. The product is packaged in a sealed carton. Under the cap and nozzle, each bottle has an aluminum seal around bottle neck. Do not use if any of these features are torn or damaged.
© 2023 Northstar Healthcare UC
Distributed by: McKesson Corp.,
via SSSL. Memphis, TN 38141
Money Back Guarantee
MH/DRUGS/25-AD/097
Rev. 08/26
NDC 70677-1319-1
FULL PRESCRIPTION STRENGTH
Allergy Symptom Reliever
Fluticasone Propionate Nasal Spray, USP
50 mcg per Spray
(Glucocorticoid)*
Non-Drowsy
24 Hour Relief of:
*Fluticasone propionate is a steroid medicine known as a glucocorticoid.
24 HOUR ALLERGY RELIEF
120 METERED SPRAYS
0.54 fl oz (15.8 mL)

| Resource | Code type | Value | Equivalent identifiers | Source image |
|---|---|---|---|---|
| Barcode | EAN-13 | 0010939962423 | GTIN-13: 0010939962423 EAN-13: 0010939962423 GTIN-12: 010939962423 UPC-A: 010939962423 GTIN storage (14 digits): 00010939962423 | carton120sprays.jpg |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 70677-1319 | 70677-1319-1 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| FLUTICASONE PROPIONATE | O2GMZ0LF5W | ACTIB |
| BENZALKONIUM CHLORIDE | F5UM2KM3W7 | IACT |
| ANHYDROUS DEXTROSE | 5SL0G7R0OK | IACT |
| MICROCRYSTALLINE CELLULOSE | OP1R32D61U | IACT |
| PHENYLETHYL ALCOHOL | ML9LGA7468 | IACT |
| POLYSORBATE 80 | 6OZP39ZG8H | IACT |
| WATER | 059QF0KO0R | IACT |
| CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED | K679OBS311 | IACT |
All distinct exact application/product contexts derived from this label’s complete NDC list are paginated below.
| Application-product | Trade name | Ingredient | Strength | Dosage form / route | TE codes | RLD / RS | Approval date |
|---|---|---|---|---|---|---|---|
| A218742-001 | FLUTICASONE PROPIONATE | FLUTICASONE PROPIONATE | 0.05MG/SPRAY | SPRAY, METERED / NASAL | 2026-03-16 |
Observed FDA ZIP history: Each table is queried independently by exact application/product key from successfully parsed Orange Book snapshots. Capture times identify archived source observations; absence or a change between snapshots is not inferred. FDA publication files that were not recoverable as structured ZIP data are not represented as states.
| Captured | Edition | Application-product | Trade name | Strength | Dosage form / route | Product TE source text | RLD / RS | Approval date | Source SHA-256 |
|---|---|---|---|---|---|---|---|---|---|
| 2026-10-15 13:18:30 | 2026-09 | A218742-001 | FLUTICASONE PROPIONATE | 0.05MG/SPRAY | SPRAY, METERED / NASAL | 2026-03-16 | c2088c7a36db… | ||
| 2026-09-14 22:38:34 | 2026-08 | A218742-001 | FLUTICASONE PROPIONATE | 0.05MG/SPRAY | SPRAY, METERED / NASAL | 2026-03-16 | 84e616aacf4f… | ||
| 2026-08-18 06:07:40 | 2026-07 | A218742-001 | FLUTICASONE PROPIONATE | 0.05MG/SPRAY | SPRAY, METERED / NASAL | 2026-03-16 | caaa826d4ba7… | ||
| 2026-07-26 02:55 UTC · 3 captures of this ZIP | 2026-06 | A218742-001 | FLUTICASONE PROPIONATE | 0.05MG/SPRAY | SPRAY, METERED / NASAL | 2026-03-16 | a50c72e98297… |
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Adverse event summaries are temporarily unavailable. Other product information remains available.