Indications and uses
Temporarily relieves these symptoms of hay fever or other upper respiratory allergies: nasal congestion runny nose sneezing itchy nose itchy, watery eyes
Allergy Relief
- Manufacturer
- CVS PHARMACY, INC
- Effective date
- 2025-08-05
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 5
- Source
- full-release
- Hydrated at
- 2026-06-01 01:09:19
Label at a glance#
ProductAllergy Relief
Active ingredientFLUTICASONE PROPIONATE
Label structure10 sections
Dosage and administration
read the Quick Start Guide for how to: prime the bottle use the spray 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 of daily use – ask ...
Storage and handling
TAMPER EVIDENT: Do not use if plastic sleeve is torn or broken. 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. 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 carton and enclosed insert. They contain important additional...
Contacts and useful links#
Label contents#
Full prescribing information#
Active ingredient (in each spray)
Fluticasone propionate (glucocorticold) 50 mcg
Purpose
Allergy symptom reliever
Uses
Temporarily relieves these symptoms of hay fever or other upper respiratory allergies:
- nasal congestion
- runny nose
- sneezing
- itchy nose
- itchy, watery eyes
Warnings
Only for use in the nose. Do not spray into your eyes or mouth.
Do not use
- in children under 4 years of age
- to treat asthma
- if you have an injury or surgery to your nose that is not fully healed
- if you have ever had an allergic reaction to this product or any of the ingredients
Ask a doctor before use if you
have or had glaucoma or cataracts
Ask a Doctor or pharmacist before use if you are taking
- medicine for HIV infection (such as ritonavir)
- a steroid medicine for asthma, allergies or skin rash
- ketoconazole pills (medicine for fungal infection)
When using this product
- the growth rate of some children may be slower
- stinging or sneezing may occur for a few seconds right after use
- do not share this bottle with anyone else as this may spread germs
- remember to tell your doctor about all the medicines you take, including this one
Stop use and ask a doctor if
- you have, or come into contact with someone who has, chicken pox, measles or tuberculosis
- your symptoms do not get better within 7 days of starting use or you get new symptoms such as severe facial pain or thick nasal discharge. You may have something more than allergies, such as an infection.
- you get a constant whistling sound from your nose. This may be a sign of damage inside your nose.
- you get an allergic reaction to this product. Seek medical help right away.
- you get new changes to your vision that develop after starting this product
- you have severe or frequent nosebleeds
If pregnant or breast-feeding,
ask a health professional before use.
Keep out of reach of children
In case of overdose, get medical help or contact a Poison Control Center (1-800-222-1222) right away
Directions
- read the Quick Start Guide for how to:
- prime the bottle
- use the spray
- 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 of daily use – ask your doctor if you can keep using
CHILDREN 4 TO 11 YEARS OF AGE
- the growth rate of some children may be slower while using this product. Children should use for the shortest amount of time necessary to achieve symptom relief. Talk to your child’s doctor if your child needs to use the spray for longer than two months a year.
- an adult should supervise use
- use 1 spray in each nostril once daily
CHILDREN UNDER 4 YEARS OF AGE
- do not use
Other information
- TAMPER EVIDENT: Do not use if plastic sleeve is torn or broken. 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.
- 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 carton and enclosed insert. They contain important additional information.
Inactive ingredient
benzalkonium chloride, carboxymethylcellulose sodium, dextrose, microcrystalline cellulose, phenylethyl alcohol, polysorbate 80, purified water
Questions or comments?
call 1-800-616-2471
Principal display panel
Compare to the active ingredient in Flonase®*
Full Prescription Strength
Non-Drowsy
Fluticasone Propionate
Nasal Spray (Glucocorticoid,
50 mcg per spray
ALLERGY SYMPTOM RELIEVER NASAL SPRAY
24 Hour relief of:
- Itchy, watery eyes
- Nasal congestion
- Runny nose
- Itchy nose
- Sneezing
METERED SPRAYS
*This product is not distributed by GlaxoSmithKline, owner of the registered trademark Flonase®.
Distributed by: CVS Pharmacy, Inc.
One CVS Drive, Woonsocket, RI 02895
Package label
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| f4fb2f5a-dadb-40e3-a4b1-a2a58f5d9a33 | Product name | 3 | 20260126 |
| 343e8617-eb68-1e10-cfa9-8c30af285764 | Product name | 3 | 20240513 |
| a31ad3df-8021-2ea1-94eb-0fe2f49b7729 | Product name | 4 | 20220719 |
| 813fe018-3e3c-40e4-8f71-7ab50f3dfe81 | Product name | 2 | 20180723 |
| 3bcd721e-0555-4bc3-96c6-690471ff9d94 | Product name | 1 | 20171113 |
| 9f9452df-fa34-43d4-97fe-c6605344c5a8 | Product name | 1 | 20171113 |
| 0e5a25a6-9f05-44b5-8449-aa63e59f7202 | Product name | 1 | 20170426 |
| f3c5232f-03de-44f5-996a-90cd9c08bc60 | Product name | 1 | 20170426 |
| 1cb17fbb-0da4-2841-37bc-e7079783e1a2 | Product name | 1 | 20140508 |
| 667f427a-8698-a508-767a-53ed61b4c2e9 | Product name | 1 | 20140508 |
| 6a97ffc8-1d4d-a971-4978-85ba3a22eac9 | Product name | 1 | 20140508 |
| 6df84e13-2223-fa46-1e26-17e2f58a1e1c | Product name | 1 | 20140508 |
| 90fec588-984c-4375-cfd4-7e40114bdf80 | Product name | 1 | 20140508 |
| 9c1d3c48-b162-204b-f55b-e0f25c31c52e | Product name | 1 | 20140508 |
| 9fdb6139-394b-1510-4baf-bde68c419789 | Product name | 1 | 20140508 |
| aef26912-037b-9a4e-db49-225ef6dfd8f1 | Product name | 1 | 20140508 |
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 51316-074-25 | Allergy Relief | 2 in 1 BOX | SPRAY, METERED | 2 | 5 | |
| 51316-074-25 | Allergy Relief | 120 in 1 BOTTLE, PLASTIC | SPRAY, METERED | 120 | 5 | |
| 51316-074-34 | Allergy Relief | 60 in 1 BOTTLE | SPRAY, METERED | 60 | 5 | |
| 51316-074-34 | Allergy Relief | 1 in 1 BOX | SPRAY, METERED | 1 | 5 | |
| 51316-074-35 | Allergy Relief | 3 in 1 BOX | SPRAY, METERED | 3 | 5 | |
| 51316-074-35 | Allergy Relief | 120 in 1 BOTTLE | SPRAY, METERED | 120 | 5 | |
| 51316-074-54 | Allergy Relief | 1 in 1 BOX | SPRAY, METERED | 1 | 5 | |
| 51316-074-54 | Allergy Relief | 120 in 1 BOTTLE | SPRAY, METERED | 120 | 5 |
Products#
Every source-derived product name is available through these pages.
- Allergy Relief
- fluticasone propionate
- FLUTICASONE
- BENZALKONIUM CHLORIDE
- DEXTROSE, UNSPECIFIED FORM
- MICROCRYSTALLINE CELLULOSE
- PHENYLETHYL ALCOHOL
- POLYSORBATE 80
- WATER
- CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 51316-074 | 51316-074-25, 51316-074-54, 51316-074-34, 51316-074-35 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| FLUTICASONE PROPIONATE | O2GMZ0LF5W | ACTIB |
| BENZALKONIUM CHLORIDE | F5UM2KM3W7 | IACT |
| DEXTROSE, UNSPECIFIED FORM | IY9XDZ35W2 | IACT |
| MICROCRYSTALLINE CELLULOSE | OP1R32D61U | IACT |
| PHENYLETHYL ALCOHOL | ML9LGA7468 | IACT |
| POLYSORBATE 80 | 6OZP39ZG8H | IACT |
| WATER | 059QF0KO0R | IACT |
| CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM | K679OBS311 | IACT |
Source Document#
openFDA label cross-check#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| 77867407-8f32-488a-8250-fb13595b309a | 196c0400-98c0-4bd2-bc2e-c09741bdc85e | 2025-08-05 | Warnings | 77867407-8f32-488a-8250-fb13595b309a 196c0400-98c0-4bd2-bc2e-c09741bdc85e |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.