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

southern cross pharma pty ltd - leflunomide, quantity: 20 mg - tablet, film coated - excipient ingredients: microcrystalline cellulose; lactose monohydrate; maize starch; povidone; crospovidone; colloidal anhydrous silica; magnesium stearate; titanium dioxide; hypromellose; purified talc; iron oxide yellow; macrogol 6000 - treatment of active rheumatoid arthritis.,treatment of active psoriatic arthritis. leflunomide is not indicated for the treatment of psoriasis that is not associated with manifestations of arthritic disease. the combined use of leflunomide with other disease modifying antirheumatic drugs (dmards) has not been adequately studied (see precautions).

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

southern cross pharma pty ltd - leflunomide, quantity: 10 mg - tablet, film coated - excipient ingredients: microcrystalline cellulose; lactose monohydrate; maize starch; povidone; crospovidone; colloidal anhydrous silica; magnesium stearate; titanium dioxide; hypromellose; macrogol 4000 - treatment of active rheumatoid arthritis.,treatment of active psoriatic arthritis. leflunomide is not indicated for the treatment of psoriasis that is not associated with manifestations of arthritic disease. the combined use of leflunomide with other disease modifying antirheumatic drugs (dmards) has not been adequately studied (see precautions).

New Zealand - English - Ministry for Primary Industries

schering-plough animal health limited - 4-androstene-3,17-dione - 4-androstene-3,17-dione 1.5 g/litre - vaccine

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

deseret biologicals, inc. - acetaldehyde (unii: go1n1zpr3b) (acetaldehyde - unii:go1n1zpr3b), dopamine hydrochloride (unii: 7l3e358n9l) (dopamine - unii:vtd58h1z2x), prasterone (unii: 459ag36t1b) (prasterone - unii:459ag36t1b), 7-keto-dehydroepiandrosterone (unii: 2334ljd2e9) (7-keto-dehydroepiandrosterone - unii:2334ljd2e9), estrone (unii: 2di9ha706a) (estrone - unii:2di9ha706a), sus scrofa ovary (unii: s7ytv04r8o) (sus scrofa ovary - unii:s7ytv04r8o), cholesterol (unii: 97c5t2uq7j) (cholesterol - unii:97c5t2uq7j), progesterone (unii: 4g7ds2q64y) (progesterone - unii:4g7ds2q64y), testosterone (unii: 3xmk78s47o) (testosterone - unii:3xmk78s47o), cortisone acetate (unii: 883wkn7w8x) (cortisone - unii:v27w9254fz), aldosterone (unii: 4964p6t9rb) (aldosterone - unii:4964p6t9rb), androsterone (unii: c24w7j5d5r) (androsterone - unii:c24w7j5d5r), follitropin (unii: 076whw89tw) (follitropin - unii:076whw89tw) - 7-oxo-dehydroepiandrosterone 3β-acetate – menstrual problems, acetaldehyde – emotional swings, aldosterone - irritability, androsterone - headache, cholesterinum – fluid retention, cortisone aceticum – food cravings, dhea – menopausal symptoms, dopamine hydrochloride – fluid retention, follicle stimulating hormone – andropausal symptoms, folliculinum – emotional swings, oophorinum - headache, progesterone – irritability, testosterone – fluid retention • for the temporary relief of symptoms including: • andropause symptoms • fluid retention • emotional swings • menstrual problems  • food craving • headache  • menopause symptoms • irritability these statements are based upon homeopathic principles. they have not been reviewed by the food and drug administration.

New Zealand - English - Medsafe (Medicines Safety Authority)

viatris limited - leflunomide 10mg - film coated tablet - 10 mg - active: leflunomide 10mg excipient: colloidal silicon dioxide crospovidone lactose magnesium stearate microcrystalline cellulose opadry white y-22-7719 povidone pregelatinised maize starch purified water - rheumatoid arthritis, to improve signs and symptoms, to retard joint destruction and to improve functional ability and quality of life. ataris may be used in patients who have failed to respond to other treatments or as a first line of treatment in patients who have a contraindication to other treatments.

New Zealand - English - Medsafe (Medicines Safety Authority)

viatris limited - leflunomide 20mg - film coated tablet - 20 mg - active: leflunomide 20mg excipient: colloidal silicon dioxide crospovidone lactose magnesium stearate microcrystalline cellulose opadry beige y-22-17165 povidone pregelatinised maize starch purified water - rheumatoid arthritis, to improve signs and symptoms, to retard joint destruction and to improve functional ability and quality of life. ataris may be used in patients who have failed to respond to other treatments or as a first line of treatment in patients who have a contraindication to other treatments.

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

viatrexx bio incorporated - androsterone (unii: c24w7j5d5r) (androsterone - unii:c24w7j5d5r), artichoke (unii: 4f3w47plbe) (artichoke - unii:4f3w47plbe), adenosine triphosphate (unii: 8l70q75fxe) (adenosine triphosphate - unii:8l70q75fxe), basic fibroblast growth factor (human) (unii: s3529g9m9v) (basic fibroblast growth factor (human) - unii:s3529g9m9v), ersofermin (unii: 1nwt5sw3nw) (ersofermin - unii:1nwt5sw3nw), adenosine cyclic phosphate (unii: e0399ozs9n) (adenosine cyclic phosphate - unii:e0399ozs9n), levocarnitine (unii: 0g389 - viatrexx-cellulite  a sterile, injectable, biodegradable, clear isotonic liquid that is injected into the various layers of the skin, adipose, cellulite, other body tissues or added to an iv, either as a push or into the bag. this product should not be used in patients with a known hypersensitivity to any ingredient found in the formula, porcine products, isotonic saline or benzyl alcohol, or patients with a history of severe allergies. as with all injections, epinephrine injection (1:1,000) must be immediately available should an acute anaphylactoid reaction occur due to any component of the injection. this product contains 1% benzyl alcohol. benzyl alcohol has been reported to be associated with a fatal "gasping syndrome" in premature infants. due to the benzyl alcohol content, this product should not be given to a pregnant woman. this product should not be used in patients with a known hypersensitivity to any ingredient in this formula, porcine products, isotonic saline or benzyl alcohol, or patients with

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

pro weight loss inc. - acetaldehyde (unii: go1n1zpr3b) (acetaldehyde - unii:go1n1zpr3b), dopamine hydrochloride (unii: 7l3e358n9l) (dopamine - unii:vtd58h1z2x), prasterone (unii: 459ag36t1b) (prasterone - unii:459ag36t1b), 7-keto-dehydroepiandrosterone (unii: 2334ljd2e9) (7-keto-dehydroepiandrosterone - unii:2334ljd2e9), estrone (unii: 2di9ha706a) (estrone - unii:2di9ha706a), sus scrofa ovary (unii: s7ytv04r8o) (sus scrofa ovary - unii:s7ytv04r8o), cholesterol (unii: 97c5t2uq7j) (cholesterol - unii:97c5t2uq7j), progesterone (unii: 4g7ds2q64y) (progesterone - unii:4g7ds2q64y), testosterone (unii: 3xmk78s47o) (testosterone - unii:3xmk78s47o), cortisone acetate (unii: 883wkn7w8x) (cortisone - unii:v27w9254fz), aldosterone (unii: 4964p6t9rb) (aldosterone - unii:4964p6t9rb), androsterone (unii: c24w7j5d5r) (androsterone - unii:c24w7j5d5r), follitropin (unii: 076whw89tw) (follitropin - unii:076whw89tw) - temporary relief of symptoms related to hormone imbalances of insufficiencies in men and women, including low energy, inability to handle stress, trouble focusing, changes in mood, infertility, irregular menstrual cycles (females), and lack of libido.** **these statements are based upon homeopathic principles. they have not been reviewed by the food and drug administration. temporary relief of symptoms related to hormone imbalances of insufficiencies in men and women, including low energy, inability to handle stress, trouble focusing, changes in mood, infertility, irregular menstrual cycles (females), and lack of libido.** **these statements are based upon homeopathic principles. they have not been reviewed by the food and drug administration.

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

viatrexx bio incorporated - androsterone (30k), artichoke (30k), atp (30k), bfgf (6x, 200k), camp (30k), l-carnitine (30k), centella asiatica (6x, 30k), citric acid (30k), cobalt (30k), estrogen (200k), ferrum fumaricum (30k), fumaric acid (30k), ginkgo (30k), hamamelis (30k), hyaluronidase (4x, 30k), il-3 (8x, 200k), kalium asparticum (30k), lactic acid (30k), lymphatic vessel (8x, 200k), melilotus (30k), mn (30k), natrum oxalaceticum (30k), natrum pyruvicum (30k), quinhydrone (30k), succinic acid (30k), vein (6x, 200k), vitamin a (3 - cellulite drainage & tonification, metabolism and lipid balance, hormonal support, circulatory support and regeneration. 

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

deseret biologicals, inc. - salsolinol hydrochloride, (+/-)- (unii: 1c0f27weal) (salsolinol hydrochloride, (+/-)- - unii:1c0f27weal), cholesterol (unii: 97c5t2uq7j) (cholesterol - unii:97c5t2uq7j), prasterone (unii: 459ag36t1b) (prasterone - unii:459ag36t1b), 7-keto-dehydroepiandrosterone (unii: 2334ljd2e9) (7-keto-dehydroepiandrosterone - unii:2334ljd2e9), estrone (unii: 2di9ha706a) (estrone - unii:2di9ha706a), sus scrofa ovary (unii: s7ytv04r8o) (sus scrofa ovary - unii:s7ytv04r8o), progesterone (unii: 4g7ds2q64y) (progestero - salsolinol hydrochloride, (+/-)- 6 [hp_x] in 1 ml - for temporary relief of symptoms related to menstrual and cyclic related conditions including emotional swings, headache, irritability, cravings and fluid retention in both menopause and andropause.** **these statements are based upon homeopathic principles. they have not been reviewed by the food and drug administration. for temporary relief of symptoms related to menstrual and cyclic related conditions including emotional swings, headache, irritability, cravings and fluid retention in both menopause and andropause.** **these statements are based upon homeopathic principles. they have not been reviewed by the food and drug administration.