can also be produced in some patients by systemic absorption of topical corticosteroids while on treatment. factors that predispose a patient using a topical corticosteroid to hpa axis suppression include the use of high potency steroids, large treatment surface areas, prolonged use, use of occlusive dressing, altered skin barrier, liver failure and young age. because of the potential for systemic absorption, use of topical corticosteroids may require that patients be periodically evaluated for hpa axis suppression. this may be done by using the adrenocorticotropic hormone (acth) stimulation test. in a study evaluating the effects of mometasone furoate lotion on the hpa axis, 15 ml were applied without occlusion twice daily (30 ml per day) for 7 days to 4 adult subjects with scalp and body psoriasis. at the end of treatment, the plasma cortisol levels for each of the 4 subjects remained within the normal range and changed little from baseline. if hpa axis suppression is documented, an attempt should be made to gradually withdraw the drug, to reduce the frequency of application, or to substitute a less potent corticosteroid. recovery of hpa axis function is generally prompt upon discontinuation of topical corticosteroids. infrequently, signs and symptoms of glucocorticosteroid insufficiency may occur, requiring supplemental systemic corticosteroids. pediatric patients may be more susceptible to systemic toxicity from equivalent doses due to their larger skin surface to body mass ratios [see use in specific populations (8.4) ] . 5.2 ophthalmic adverse reactions use of topical corticosteroids may increase the risk of posterior subcapsular cataracts and glaucoma. cataracts and glaucoma have been reported in postmarketing experience with the use of topical corticosteroid products, including the topical mometasone products [see adverse reactions (6.2) ] . avoid contact of mometasone furoate lotion (mometasone furoate topical solution 0.1%) with eyes. advise patients to report any visual symptoms and consider referral to an ophthalmologist for evaluation. 5.3 allergic contact dermatitis if irritation develops, mometasone furoate lotion (mometasone furoate topical solution 0.1%) should be discontinued and appropriate therapy instituted. allergic contact dermatitis with corticosteroids is usually diagnosed by observing failure to heal rather than noting a clinical exacerbation. such an observation should be corroborated with appropriate diagnostic patch testing. 5.4 concomitant skin infections if concomitant skin infections are present or develop, an appropriate antifungal or antibacterial agent should be used. if a favorable response does not occur promptly, use of mometasone furoate lotion (mometasone furoate topical solution 0.1%) should be discontinued until the infection has been adequately controlled.

n. • apply a few drops to the affected skin areas once daily and massage lightly until it disappears. ( 2 ) • discontinue therapy when control is achieved. ( 2 ) • if no improvement is seen within 2 weeks, reassess diagnosis. ( 2 ) • do not use with occlusive dressings unless directed by a physician. ( 2 )

o be possibly or probably related to treatment with mometasone furoate lotion (mometasone furoate topical solution 0.1%) during a clinical trial in 14% of 65 pediatric subjects 6 months to 2 years of age: decreased glucocorticoid levels, 4; paresthesia, 2; dry mouth,1; an unspecified endocrine disorder, 1; pruritus, 1; and an unspecified skin disorder, 1. the following signs of skin atrophy were also observed among 65 subjects treated with mometasone furoate lotion (mometasone furoate topical solution 0.1%) in a clinical trial: shininess, 4; telangiectasia, 2; loss of elasticity, 2; and loss of normal skin markings, 3. 6.2 postmarketing experience because adverse reactions are reported voluntarily from a population of uncertain size, it is not always possible to reliably estimate their frequency or establish a causal relationship to drug exposure. postmarketing reports for local adverse reactions to topical corticosteroids include irritation, dryness, folliculitis, hypertrichosis, acneiform eruptions, hypopigmentation, perioral dermatitis, allergic contact dermatitis, secondary infection, skin atrophy, striae, and miliaria. these adverse reactions may occur more frequently with the use of occlusive dressings. postmarketing reports for ophthalmic adverse reactions to topical corticosteroids include blurred vision, cataracts, glaucoma, increased intraocular pressure, and central serous chorioretinopathy.

doses of 60 mcg/kg and above. fetal survival was reduced at 180 mcg/kg. no toxicity was observed at 20 mcg/kg. (doses of 20, 60, and 180 mcg/kg in the mouse are approximately 0.01, 0.02, and 0.05 times the estimated maximum clinical topical dose from mometasone furoate lotion (mometasone furoate topical solution 0.1%) on a mcg/m 2 basis.) in rats, mometasone furoate produced umbilical hernias at topical doses of 600 mcg/kg and above. a dose of 300 mcg/kg produced delays in ossification, but no malformations. (doses of 300 and 600 mcg/kg in the rat are approximately 0.2 and 0.4 times the estimated maximum clinical topical dose from mometasone furoate lotion (mometasone furoate topical solution 0.1%) on a mcg/m 2 basis.) in rabbits, mometasone furoate caused multiple malformations (e.g., flexed front paws, gallbladder agenesis, umbilical hernia, hydrocephaly) at topical doses of 150 mcg/kg and above (approximately 0.2 times the estimated maximum clinical topical dose from mometasone furoate lotion (mometasone furoate topical solution 0.1%) on a mcg/m 2 basis). in an oral study, mometasone furoate increased resorptions and caused cleft palate and/or head malformations (hydrocephaly and domed head) at 700 mcg/kg. at 2,800 mcg/kg most litters were aborted or resorbed. no toxicity was observed at 140 mcg/kg. (doses at 140, 700, and 2,800 mcg/kg in the rabbit are approximately 0.2, 0.9, and 3.6 times the estimated maximum clinical topical dose from mometasone furoate lotion (mometasone furoate topical solution 0.1%) on a mcg/m 2 basis.) when rats received subcutaneous doses of mometasone furoate throughout pregnancy or during the later stages of pregnancy, 15 mcg/kg caused prolonged and difficult labor and reduced the number of live births, birth weight, and early pup survival. similar effects were not observed at 7.5 mcg/kg. (doses of 7.5 and 15 mcg/kg in the rat are approximately 0.005 and 0.01 times the estimated maximum clinical topical dose from mometasone furoate lotion (mometasone furoate topical solution 0.1%) on a mcg/m 2 basis.) 8.3 nursing mothers systemically administered corticosteroids appear in human milk and could suppress growth, interfere with endogenous corticosteroid production, or cause other untoward effects. it is not known whether topical administration of corticosteroids could result in sufficient systemic absorption to produce detectable quantities in human milk. because many drugs are excreted in human milk, caution should be exercised when mometasone furoate lotion (mometasone furoate topical solution 0.1%) is administered to a nursing woman. 8.4 pediatric use since safety and efficacy of mometasone furoate lotion (mometasone furoate topical solution 0.1%) have not been established in pediatric patients below 12 years of age, its use in this age group is not recommended. mometasone furoate lotion (mometasone furoate topical solution 0.1%) caused hpa axis suppression in approximately 29% of pediatric subjects ages 6 to 23 months, who showed normal adrenal function by cortrosyn test before starting treatment, and were treated for approximately 3 weeks over a mean body surface area of 40% (range 16% to 90%). the criteria for suppression were: basal cortisol level of ≤ 5 mcg/dl, 30-minute post-stimulation level of ≤ 18 mcg/dl, or an increase of <7 mcg/dl. follow-up testing 2 to 4 weeks after stopping treatment, available for 8 of the subjects, demonstrated suppressed hpa axis function in 1 subject, using these same criteria. long-term use of topical corticosteroids has not been studied in this population [see clinical pharmacology (12.2) ] . because of a higher ratio of skin surface area to body mass, pediatric patients are at a greater risk than adults of hpa axis suppression and cushing's syndrome when they are treated with topical corticosteroids. they are, therefore, also at greater risk of adrenal insufficiency during and/or after withdrawal of treatment. pediatric patients may be more susceptible than adults to skin atrophy, including striae, when they are treated with topical corticosteroids. pediatric patients applying topical corticosteroids to greater than 20% of body surface are at higher risk of hpa axis suppression. hpa axis suppression, cushing's syndrome, linear growth retardation, delayed weight gain, and intracranial hypertension have been reported in pediatric patients receiving topical corticosteroids. manifestations of adrenal suppression in children include low plasma cortisol levels and absence of response to acth stimulation. manifestations of intracranial hypertension include bulging fontanelles, headaches, and bilateral papilledema. mometasone furoate lotion (mometasone furoate topical solution 0.1%) should not be used in the treatment of diaper dermatitis. 8.5 geriatric use clinical trials of mometasone furoate lotion (mometasone furoate topical solution 0.1%) did not include sufficient numbers of subjects aged 65 and over to determine whether they respond differently from younger subjects. other reported clinical experience has not identified differences in responses between the elderly and younger patients. in general, dose selection for an elderly patient should be cautious usually starting at the low end of the dosing range.

fetal survival was reduced at 180 mcg/kg. no toxicity was observed at 20 mcg/kg. (doses of 20, 60, and 180 mcg/kg in the mouse are approximately 0.01, 0.02, and 0.05 times the estimated maximum clinical topical dose from mometasone furoate lotion (mometasone furoate topical solution 0.1%) on a mcg/m 2 basis.) in rats, mometasone furoate produced umbilical hernias at topical doses of 600 mcg/kg and above. a dose of 300 mcg/kg produced delays in ossification, but no malformations. (doses of 300 and 600 mcg/kg in the rat are approximately 0.2 and 0.4 times the estimated maximum clinical topical dose from mometasone furoate lotion (mometasone furoate topical solution 0.1%) on a mcg/m 2 basis.) in rabbits, mometasone furoate caused multiple malformations (e.g., flexed front paws, gallbladder agenesis, umbilical hernia, hydrocephaly) at topical doses of 150 mcg/kg and above (approximately 0.2 times the estimated maximum clinical topical dose from mometasone furoate lotion (mometasone furoate topical solution 0.1%) on a mcg/m 2 basis). in an oral study, mometasone furoate increased resorptions and caused cleft palate and/or head malformations (hydrocephaly and domed head) at 700 mcg/kg. at 2,800 mcg/kg most litters were aborted or resorbed. no toxicity was observed at 140 mcg/kg. (doses at 140, 700, and 2,800 mcg/kg in the rabbit are approximately 0.2, 0.9, and 3.6 times the estimated maximum clinical topical dose from mometasone furoate lotion (mometasone furoate topical solution 0.1%) on a mcg/m 2 basis.) when rats received subcutaneous doses of mometasone furoate throughout pregnancy or during the later stages of pregnancy, 15 mcg/kg caused prolonged and difficult labor and reduced the number of live births, birth weight, and early pup survival. similar effects were not observed at 7.5 mcg/kg. (doses of 7.5 and 15 mcg/kg in the rat are approximately 0.005 and 0.01 times the estimated maximum clinical topical dose from mometasone furoate lotion (mometasone furoate topical solution 0.1%) on a mcg/m 2 basis.)

pharmacology (12.2) ] . because of a higher ratio of skin surface area to body mass, pediatric patients are at a greater risk than adults of hpa axis suppression and cushing's syndrome when they are treated with topical corticosteroids. they are, therefore, also at greater risk of adrenal insufficiency during and/or after withdrawal of treatment. pediatric patients may be more susceptible than adults to skin atrophy, including striae, when they are treated with topical corticosteroids. pediatric patients applying topical corticosteroids to greater than 20% of body surface are at higher risk of hpa axis suppression. hpa axis suppression, cushing's syndrome, linear growth retardation, delayed weight gain, and intracranial hypertension have been reported in pediatric patients receiving topical corticosteroids. manifestations of adrenal suppression in children include low plasma cortisol levels and absence of response to acth stimulation. manifestations of intracranial hypertension include bulging fontanelles, headaches, and bilateral papilledema. mometasone furoate lotion (mometasone furoate topical solution 0.1%) should not be used in the treatment of diaper dermatitis.

olution 0.1%) on the hpa axis, 15 ml were applied without occlusion twice daily (30 ml per day) for 7 days to 4 adult subjects with scalp and body psoriasis. at the end of treatment, the plasma cortisol levels for each of the 4 subjects remained within the normal range and changed little from baseline [see warnings and precautions (5.1) ] . sixty-five pediatric subjects ages 6 to 23 months, with atopic dermatitis, were enrolled in an open-label, hpa axis safety trial. mometasone furoate lotion (mometasone furoate topical solution 0.1%) was applied once daily for approximately 3 weeks over a mean body surface area of 40% (range 16% to 90%). in approximately 29% of subjects who showed normal adrenal function by cortrosyn test before starting treatment, adrenal suppression was observed at the end of treatment with mometasone furoate lotion (mometasone furoate topical solution, 0.1%). the criteria for suppression were: basal cortisol level of ≤ 5 mcg/dl, 30-minute post-stimulation level of ≤ 18 mcg/dl, or an increase of <7 mcg/dl. follow-up testing 2 to 4 weeks after stopping treatment, available for 8 of the subjects, demonstrated suppressed hpa axis function in 1 subject, using these same criteria [see use in specific populations (8.4) ] . 12.3 pharmacokinetics the extent of percutaneous absorption of topical corticosteroids is determined by many factors including the vehicle and the integrity of the epidermal barrier. studies in humans indicate that approximately 0.7% of the applied dose of mometasone furoate lotion (mometasone furoate topical solution 0.1%) enters the circulation after 8 hours of contact on normal skin without occlusion. a similar minimal degree of absorption of the corticosteroid from the lotion formulation would be anticipated. inflammation and/or other disease processes in the skin may increase percutaneous absorption.

furoate topical solution 0.1%) on a mcg/m 2 basis). mometasone furoate increased chromosomal aberrations in an in vitro chinese hamster ovary cell assay, but did not increase chromosomal aberrations in an in vitro chinese hamster lung cell assay. mometasone furoate was not mutagenic in the ames test or mouse lymphoma assay, and was not clastogenic in an in vivo mouse micronucleus assay, a rat bone marrow chromosomal aberration assay, or a mouse male germ-cell chromosomal aberration assay. mometasone furoate also did not induce unscheduled dna synthesis in vivo in rat hepatocytes. in reproductive studies in rats, impairment of fertility was not produced in male or female rats by subcutaneous doses up to 15 mcg/kg (approximately 0.01 times the estimated maximum clinical topical dose from mometasone furoate lotion (mometasone furoate topical solution 0.1%) on a mcg/m 2 basis).

.1%) on a mcg/m 2 basis). mometasone furoate increased chromosomal aberrations in an in vitro chinese hamster ovary cell assay, but did not increase chromosomal aberrations in an in vitro chinese hamster lung cell assay. mometasone furoate was not mutagenic in the ames test or mouse lymphoma assay, and was not clastogenic in an in vivo mouse micronucleus assay, a rat bone marrow chromosomal aberration assay, or a mouse male germ-cell chromosomal aberration assay. mometasone furoate also did not induce unscheduled dna synthesis in vivo in rat hepatocytes. in reproductive studies in rats, impairment of fertility was not produced in male or female rats by subcutaneous doses up to 15 mcg/kg (approximately 0.01 times the estimated maximum clinical topical dose from mometasone furoate lotion (mometasone furoate topical solution 0.1%) on a mcg/m 2 basis).

ent of diaper dermatitis. do not apply mometasone furoate lotion (mometasone furoate topical solution 0.1%) in the diaper area, as diapers or plastic pants may constitute occlusive dressing. • discontinue therapy when control is achieved. if no improvement is seen within 2 weeks, contact the physician. • do not use other corticosteroid-containing products with mometasone furoate lotion (mometasone furoate topical solution 0.1%) without first consulting with the physician.