Nuova Zelanda - inglese - Medsafe (Medicines Safety Authority)

alcon laboratories (australia) pty ltd - carbomer 980, hypromellose - ophthalmic gel

Nuova Zelanda - inglese - Ministry for Primary Industries

dechra veterinary products nz limited - fusidic acid hemi hydrate; betamethasone - fusidic acid hemi hydrate 5 g/litre; betamethasone 1 g/litre - antibiotic

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

lawley pharmaceuticals pty ltd - testosterone, quantity: 10 mg/ml - cream - excipient ingredients: almond oil; butylated hydroxytoluene; carbomer 940; cetomacrogol 1000; cetostearyl alcohol; citric acid; dl-alpha-tocopheryl acetate; trolamine; purified water; phenoxyethanol; propyl hydroxybenzoate; ethyl hydroxybenzoate; isobutyl hydroxybenzoate; butyl hydroxybenzoate; methyl hydroxybenzoate - androfeme 1 is indicated for the treatment of hypoactive sexual desire dysfunction (hsdd) in postmenopausal women. therapeutic intervention with androfeme 1 should only be initiated in women following failure of appropriate education and correction of modifiable biopsychosocial factors (which may include neuroendocrine imbalance, physical ill health or disease, interpersonal difficulties, psychological distress or specific cultural or religious beliefs), according to the international society for the study of women?s sexual health (isswsh) process of care (see figure 1).

Irlanda - inglese - HPRA (Health Products Regulatory Authority)

reckitt's (ireland) limited - carbomer carbenoxolone sodium -

Irlanda - inglese - HPRA (Health Products Regulatory Authority)

dispersa (uk) ltd - carbomer cetrimonium bromide sorbitol edetate disodium sodium hydroxide - gel

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

organon pharma pty ltd - betamethasone dipropionate, quantity: 0.64 mg/g (equivalent: betamethasone, qty 0.5 mg/g) - lotion - excipient ingredients: carbomer 1342; isopropyl alcohol; purified water; sodium hydroxide - indications as at 22 november 1995: diprosone is indicated for the relief of the inflammatory and pruritic manifestations of corticosteroid-responsive dermatoses. these include atopic eczema, infantile eczema, nummular eczema, contact dermatitis, neurodermatitis, anogenital and senile pruritus, lichen planus, intertrigo and psoriasis. diprosone lotion is indicated wherever hair impedes access to the skin in the treatment of corticosteroid-responsive dermatoses particularly on the scalp, chest and underarms, etc. it is also indicated in the treatment of seborrhoea and psoriasis of the scalp.

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

organon pharma pty ltd - betamethasone dipropionate, quantity: 0.64 mg/g (equivalent: betamethasone, qty 0.5 mg/g) - cream - excipient ingredients: sodium hydroxide; titanium dioxide; purified water; carbomer 980; propylene glycol - for the relief of the inflammatory and pruritic manifestations of resistant or severe corticosteroid responsive dermatoses. these include atopic eczema, nummular eczema, contact dermatitis, neurodermatitis, anogenital and senile pruritus, lichen planus and psoriasis.

Nuova Zelanda - inglese - Medsafe (Medicines Safety Authority)

teva pharma (new zealand) limited - testosterone 1.41%{relative} (12.2mg/system);   - transdermal patch - 12.2 mg - active: testosterone 1.41%{relative} (12.2mg/system)   excipient: ethanol glycerol glyceryl mono-oleate carbomer copolymer (type b) methyl laurate purified water sodium hydroxide - androderm® is indicated for testosterone replacement therapy for confirmed testosterone deficiency in males.

Nuova Zelanda - inglese - Medsafe (Medicines Safety Authority)

teva pharma (new zealand) limited - testosterone 24.3mg;   - transdermal patch - 24.3 mg - active: testosterone 24.3mg   excipient: ethanol glycerol glycerol mono-oleate carbomer copolymer type b methyl laurate purified water sodium hydroxide - androderm® is indicated for testosterone replacement therapy for confirmed testosterone deficiency in males.

Nuova Zelanda - inglese - Medsafe (Medicines Safety Authority)

onelink - nifedipine 30mg;  ;   - modified release tablet - 30 mg - active: nifedipine 30mg     excipient: carbomer 934p colloidal silicon dioxide hypromellose   iron oxide red lactose monohydrate macrogol 4000 magnesium stearate   methacrylic acid copolymer povidone purified talc   titanium dioxide - treatment of mild to moderate hypertension.