NDC 0135-0615

FLONASE SENSIMIST ALLERGY RELIEF

Fluticasone Furoate

FLONASE SENSIMIST ALLERGY RELIEF is a Nasal Spray, Metered in the Human Otc Drug category. It is labeled and distributed by Glaxosmithkline Consumer Healthcare Holdings (us) Llc. The primary component is Fluticasone Furoate.

Product ID0135-0615_04e9be44-1635-43e6-92cb-b542f4486443
NDC0135-0615
Product TypeHuman Otc Drug
Proprietary NameFLONASE SENSIMIST ALLERGY RELIEF
Generic NameFluticasone Furoate
Dosage FormSpray, Metered
Route of AdministrationNASAL
Marketing Start Date2017-02-01
Marketing CategoryNDA / NDA
Application NumberNDA022051
Labeler NameGlaxoSmithKline Consumer Healthcare Holdings (US) LLC
Substance NameFLUTICASONE FUROATE
Active Ingredient Strength28 ug/1
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 0135-0615-01

1 BOTTLE in 1 CARTON (0135-0615-01) > 30 SPRAY, METERED in 1 BOTTLE
Marketing Start Date2017-02-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0135-0615-06 [00135061506]

FLONASE SENSIMIST ALLERGY RELIEF SPRAY, METERED
Marketing CategoryNDA
Application NumberNDA022051
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-01-22

NDC 0135-0615-02 [00135061502]

FLONASE SENSIMIST ALLERGY RELIEF SPRAY, METERED
Marketing CategoryNDA
Application NumberNDA022051
Product TypeHUMAN OTC DRUG
Billing UnitML
Marketing Start Date2017-02-01

NDC 0135-0615-01 [00135061501]

FLONASE SENSIMIST ALLERGY RELIEF SPRAY, METERED
Marketing CategoryNDA
Application NumberNDA022051
Product TypeHUMAN OTC DRUG
Marketing Start Date2017-02-01

NDC 0135-0615-04 [00135061504]

FLONASE SENSIMIST ALLERGY RELIEF SPRAY, METERED
Marketing CategoryNDA
Application NumberNDA022051
Product TypeHUMAN OTC DRUG
Billing UnitML
Marketing Start Date2017-02-01

NDC 0135-0615-03 [00135061503]

FLONASE SENSIMIST ALLERGY RELIEF SPRAY, METERED
Marketing CategoryNDA
Application NumberNDA022051
Product TypeHUMAN OTC DRUG
Billing UnitML
Marketing Start Date2017-02-01

NDC 0135-0615-05 [00135061505]

FLONASE SENSIMIST ALLERGY RELIEF SPRAY, METERED
Marketing CategoryNDA
Application NumberNDA022051
Product TypeHUMAN OTC DRUG
Billing UnitML
Marketing Start Date2017-07-01

Drug Details

Active Ingredients

IngredientStrength
FLUTICASONE FUROATE27.5 ug/1

OpenFDA Data

SPL SET ID:107100af-7ca2-44e8-b067-c0ab0a19a6dc
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1797890
  • 1869712
  • NDC Crossover Matching brand name "FLONASE SENSIMIST ALLERGY RELIEF" or generic name "Fluticasone Furoate"

    NDCBrand NameGeneric Name
    0173-0874Arnuity Elliptafluticasone furoate
    0173-0876Arnuity Elliptafluticasone furoate
    0173-0888Arnuity Elliptafluticasone furoate
    0135-0615FLONASE SENSIMISTfluticasone furoate
    0135-0616FLONASE SENSIMISTfluticasone furoate
    50090-5967FLONASE SENSIMISTfluticasone furoate
    50090-6075FLONASE SENSIMISTfluticasone furoate
    0173-0753VERAMYSTfluticasone furoate

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