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Fluticasone propionate (Cipla-fluticasone Dp-caps, Flohale Dp-caps, Flomist, Cipla-fluticasone Aqueous Nasal)

Fluticasone propionate

Cipla Medpro (Pty) Ltd

Registration

Applicant
Cipla Medpro (Pty) Ltd
Registrations
8

Variants

ProductStrength and formRegistrationStatusScheduleLeaflets
Cipla-fluticasone 50 dp-caps

EACH CAPSULE CONTAINS FLUTICASONE PROPIONATE 50,0 ug

5037014637/21.5.1/0146CancelledNot determinedNone
Cipla-fluticasone 100 dp-caps

EACH CAPSULE CONTAINS FLUTICASONE PROPIONATE 100,0 ug

10037014737/21.5.1/0147CancelledNot determinedNone
Cipla-fluticasone 250 dp-caps

EACH CAPSULE CONTAINS FLUTICASONE PROPIONATE 250,0 ug

25037014837/21.5.1/0148CancelledNot determinedNone
Flohale 50 dp-caps

EACH CAPSULE CONTAINS FLUTICASONE PROPIONATE 50,0 ug

5037014937/21.5.1/0149CancelledNot determinedNone
Flohale 100 dp-caps

EACH CAPSULE CONTAINS FLUTICASONE PROPIONATE 100,0 ug

10037015037/21.5.1/0150CancelledNot determinedNone
Flohale 250 dp-caps

EACH CAPSULE CONTAINS FLUTICASONE PROPIONATE 250,0 ug

25037015137/21.5.1/0151CancelledNot determinedNone
Flomist

EACH METERED SPRAY CONTAINS FLUTICASONE PROPIONATE 50,0 ug

Not listed37028937/21.5.1/0289RegisteredNot determinedNone
Cipla-fluticasone aqueous nasal spray

EACH METERED SPRAY CONTAINS FLUTICASONE PROPIONATE 50,0 ug

Spray37029037/21.5.1/0290CancelledNot determinedNone

Regulatory status

This product is still scheduled by law even when this site could not determine which tier it falls under. The label carries the S number in a square border; ask a pharmacist if you need to know its schedule.

Listings for this ingredient that could not be applied to this product

  • S4: Fluticasone propionate

    • when intended for nasal administration as an aqueous spray, in the short-term (less than 6 months prophylaxis and treatment of the symptoms of seasonal allergic rhinitis (hay fever) in adults and children over 12 years of age, subject to- (i) a maximum daily dose of 100 micrograms per nostril; and (ii) a maximum pack size of 120 doses. (S2)
    • when intended for inhalation or nasal administration. (S3)

    Consolidated Schedules 06 July 2026, lines 6423 to 6433

  • S3: Fluticasone propionate

    • when intended for inhalation or nasal administration;
    • except when intended for nasal administration as an aqueous spray in the short-term (less than 6 months prophylaxis and treatment of the symptoms of seasonal allergic rhinitis (hay fever) in adults and children over 12 years of age, subject to- (i) a maximum daily dose of 100 micrograms per nostril; and (ii) a maximum pack size of 120 doses. (S2)
    • except when intended for administration other than by inhalation or nasal administration. (S4)

    Consolidated Schedules 06 July 2026, lines 3641 to 3653

  • S2: Fluticasone propionate

    • when intended for nasal administration, as an aqueous spray, in the short-term (less than 6 months) prophylaxis and treatment of symptoms of seasonal allergic rhinitis (hay fever) in adults and children over 12 years of age, subject to- (i) a maximum daily dose of 100 micrograms per nostril; (ii) and a maximum pack size limit of 120 doses; (S3)
    • except when intended for administration other than by inhalation or nasal administration. (S4)

    Consolidated Schedules 06 July 2026, lines 2042 to 2052

This is an informational summary of the Medicines and Related Substances Act 101 of 1965 and its 2017 General Regulations. It is not medical advice and not legal advice. Always check the medicine's label, which carries the schedule number inside a square border, or ask a pharmacist if you are unsure.

C25H31F3O5S500.60 g/mol

[(6S,8S,9R,10S,11S,13S,14S,16R,17R)-6,9-Difluoro-17-(fluoromethylsulfanylcarbonyl)-11-hydroxy-10,13,16-trimethyl-3-oxo-6,7,8,11,12,14,15,16-octahydrocyclopenta[a]phenanthren-17-yl] propanoate

Drag to rotate. Structure from PubChem CID 444036.

SAHPRA documents

SAHPRA has not published a professional information or patient information leaflet for this product.

Background

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Research articles

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