Australia - English - Department of Health (Therapeutic Goods Administration)

sanofi-aventis healthcare pty ltd t/a sanofi consumer healthcare - fexofenadine hydrochloride, quantity: 6 mg/ml - oral liquid, suspension - excipient ingredients: xanthan gum; disodium edetate; titanium dioxide; propylene glycol; sucrose; purified water; monobasic sodium phosphate monohydrate; poloxamer; potassium sorbate; xylitol; dibasic sodium phosphate monohydrate; flavour - relief of symptoms associated with seasonal allergic rhinitis and allergic rhinitis in adults and children from 2 years of age. relief of symptoms associated,with urticaria in adults and children from 6 months of age.

New Zealand - English - Medsafe (Medicines Safety Authority)

viatris limited - fexofenadine hydrochloride 120mg - film coated tablet - 120 mg - active: fexofenadine hydrochloride 120mg excipient: croscarmellose sodium magnesium stearate maize starch microcrystalline cellulose opadry pink 03c54667 povidone purified water - relief of symptoms associated with seasonal allergic rhinitis in adults and children aged 12 years or older.

New Zealand - English - Medsafe (Medicines Safety Authority)

viatris limited - fexofenadine hydrochloride 180mg - film coated tablet - 180 mg - active: fexofenadine hydrochloride 180mg excipient: croscarmellose sodium magnesium stearate maize starch microcrystalline cellulose opadry yellow 03c52662 povidone - relief of symptoms associated with seasonal allergic rhinitis or urticaria in adults and children aged 12 years or older.

New Zealand - English - Medsafe (Medicines Safety Authority)

viatris limited - fexofenadine hydrochloride 30mg - film coated tablet - 30 mg - active: fexofenadine hydrochloride 30mg excipient: croscarmellose sodium magnesium stearate maize starch microcrystalline cellulose opadry pink 03c54667 povidone purified water - relief of symptoms associated with seasonal allergic rhinitis in children aged 6 to 11 years.

New Zealand - English - Medsafe (Medicines Safety Authority)

viatris limited - fexofenadine hydrochloride 60mg - film coated tablet - 60 mg - active: fexofenadine hydrochloride 60mg excipient: croscarmellose sodium magnesium stearate maize starch microcrystalline cellulose opadry yellow 03c52662 povidone purified water - relief of symptoms associated with allergic rhinitis in adults and children aged 12 years or older.

Ireland - English - HPRA (Health Products Regulatory Authority)

chanelle medical unlimited company - fexofenadine hydrochloride - film-coated tablet - 120 milligram(s) - other antihistamines for systemic use; fexofenadine

Ireland - English - HPRA (Health Products Regulatory Authority)

chanelle medical unlimited company - fexofenadine hydrochloride - film-coated tablet - 180 milligram(s) - other antihistamines for systemic use; fexofenadine

United States - English - NLM (National Library of Medicine)

bryant ranch prepack - fexofenadine hydrochloride (unii: 2s068b75zu) (fexofenadine - unii:e6582loh6v) - fexofenadine hydrochloride 180 mg

United States - English - NLM (National Library of Medicine)

mylan pharmaceuticals inc. - fexofenadine hydrochloride (unii: 2s068b75zu) (fexofenadine - unii:e6582loh6v) - fexofenadine hydrochloride 60 mg - antihistamine temporarily relieves these symptoms due to hay fever or other upper respiratory allergies:

United States - English - NLM (National Library of Medicine)

golden state medical supply, inc. - fexofenadine hydrochloride (unii: 2s068b75zu) (fexofenadine - unii:e6582loh6v) - fexofenadine hydrochloride 60 mg