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

energique, inc. - serotonin hydrochloride (unii: gkn429m9vs) (serotonin - unii:333do1rdjy), oxitriptan (unii: c1ljo185q9) (oxitriptan - unii:c1ljo185q9), acetaldehyde (unii: go1n1zpr3b) (acetaldehyde - unii:go1n1zpr3b), acetylcholine chloride (unii: af73293c2r) (acetylcholine - unii:n9yns0m02x), apiole (parsley) (unii: qq67504pxo) (apiole (parsley) - unii:qq67504pxo), ascorbic acid (unii: pq6ck8pd0r) (ascorbic acid - unii:pq6ck8pd0r), aspartame (unii: z0h242bbr1) (aspartame - unii:z0h242bbr1), butylated hydroxytoluene - may temporarily relieve symptoms associated with sensitivities to allergic responses.** **claims based on traditional homeopathic practice, not accepted medical evidence. not fda evaluated. may temporarily relieve symptoms associated with sensitivities to allergic responses.** **claims based on traditional homeopathic practice, not accepted medical evidence. not fda evaluated.

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

energique, inc. - serotonin hydrochloride (unii: gkn429m9vs) (serotonin - unii:333do1rdjy), oxitriptan (unii: c1ljo185q9) (oxitriptan - unii:c1ljo185q9), acetaldehyde (unii: go1n1zpr3b) (acetaldehyde - unii:go1n1zpr3b), acetylcholine chloride (unii: af73293c2r) (acetylcholine - unii:n9yns0m02x), apiole (parsley) (unii: qq67504pxo) (apiole (parsley) - unii:qq67504pxo), ascorbic acid (unii: pq6ck8pd0r) (ascorbic acid - unii:pq6ck8pd0r), aspartame (unii: z0h242bbr1) (aspartame - unii:z0h242bbr1), butylated hydroxytoluene - may temporarily relieve symptoms associated with sensitivities due to allergic responses.** **claims based on traditional homeopathic practice, not accepted medical evidence. not fda evaluated. may temporarily relieve symptoms associated with sensitivities due to allergic responses.** **claims based on traditional homeopathic practice, not accepted medical evidence. not fda evaluated.

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centurion labs, llc - omega-3 fatty acids (unii: 71m78end5s) (omega-3 fatty acids - unii:71m78end5s), thiamine mononitrate (unii: 8k0i04919x) (thiamine ion - unii:4abt0j945j), riboflavin (unii: tlm2976ofr) (riboflavin - unii:tlm2976ofr), pyridoxine hydrochloride (unii: 68y4cf58bv) (pyridoxine - unii:kv2jz1bi6z), cyanocobalamin (unii: p6yc3eg204) (cyanocobalamin - unii:p6yc3eg204), folic acid (unii: 935e97boy8) (folic acid - unii:935e97boy8), cholecalciferol (unii: 1c6v77qf41) (cholecalciferol - unii:1c6v77qf41), ascorbic acid (unii: pq6ck8pd0r) (ascorbic acid - unii:pq6ck8pd0r), .alpha.-tocopherol, d- (unii: n9pr3490h9) (.alpha.-tocopherol, d- - unii:n9pr3490h9), cupric sulfate (unii: lrx7aj16dt) (cupric cation - unii:8cbv67279l), zinc oxide (unii: soi2loh54z) (zinc cation - unii:13s1s8sf37), ferrous fumarate (unii: r5l488ry0q) (ferrous cation - unii:gw89581owr), magnesium (unii: i38zp9992a) (magnesium - unii:i38zp9992a) - omega-3 fatty acids 200 mg - indications and usage: c-nate dha is a prescription multivitamin/multimineral indicated for use in improving the nutritional status of women prior to conception, throughout pregnancy and in the postnatal period for both lactating and nonlactating mothers. contraindications: c-nate dha should not be used by patients with known history of hypersensitivity to any of the listed ingredients. pediatric use: safety and effectiveness in pediactric patients has not been established. geriactric use: no clinical studies have been performed in patients over 65 to determine whether older persons respond differently from younger persons. physicians should consider that elderly person may have decreased hepatic, renal, or cardiac function.

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deseret biologicals, inc. - ascorbic acid (unii: pq6ck8pd0r) (ascorbic acid - unii:pq6ck8pd0r), pyridoxine hydrochloride (unii: 68y4cf58bv) (pyridoxine - unii:kv2jz1bi6z), riboflavin (unii: tlm2976ofr) (riboflavin - unii:tlm2976ofr), lactic acid, l- (unii: f9s9ffu82n) (lactic acid, l- - unii:f9s9ffu82n), thiamine hydrochloride (unii: m572600e5p) (thiamine ion - unii:4abt0j945j), acetaldehyde (unii: go1n1zpr3b) (acetaldehyde - unii:go1n1zpr3b), prasterone (unii: 459ag36t1b) (prasterone - unii:459ag36t1b), phlorizin (unii: cu9s17279x) ( - ascorbic acid 6 [hp_x] in 1 ml - for temporary relief of symptoms related to high blood sugar including dry mouth, thirst, excess urination, night sweats, sugar and carb cravings.** **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 high blood sugar including dry mouth, thirst, excess urination, night sweats, sugar and carb cravings.** **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)

deseret biologicals, inc. - ascorbic acid (unii: pq6ck8pd0r) (ascorbic acid - unii:pq6ck8pd0r), pyridoxine hydrochloride (unii: 68y4cf58bv) (pyridoxine - unii:kv2jz1bi6z), riboflavin (unii: tlm2976ofr) (riboflavin - unii:tlm2976ofr), lactic acid, l- (unii: f9s9ffu82n) (lactic acid, l- - unii:f9s9ffu82n), thiamine hydrochloride (unii: m572600e5p) (thiamine ion - unii:4abt0j945j), acetaldehyde (unii: go1n1zpr3b) (acetaldehyde - unii:go1n1zpr3b), prasterone (unii: 459ag36t1b) (prasterone - unii:459ag36t1b), insulin pork (unii: avt680jb39 - ascorbic acid 6 [hp_x] in 1 ml - for temporary relief of symptoms related to high blood sugar including dry mouth, thirst, excess urination, night sweats, sugar and carb cravings. for temporary relief of symptoms related to high blood sugar including dry mouth, thirst, excess urination, night sweats, sugar and carb cravings.

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

mcguff pharmaceuticals, inc. - ascorbic acid (unii: pq6ck8pd0r) (ascorbic acid - unii:pq6ck8pd0r) - ascorbic acid 500 mg in 1 ml - ascor is vitamin c indicated for the short term (up to 1 week) treatment of scurvy in adult and pediatric patients age 5 months and older for whom oral administration is not possible, insufficient or contraindicated. limitations of use ascor is not indicated for treatment of vitamin c deficiency that is not associated with signs and symptoms of scurvy. none. use in specific populations 8.1 pregnancy 8.2 lactation 8.4 pediatric use 8.5 geriatric use 8.6 renal impairment 8.1 pregnancy risk summary there are no available data on use of ascor in pregnant women to inform a drug-associated risk of adverse developmental outcomes; however, use of ascorbic acid (vitamin c) has been used during pregnancy for several decades and no adverse developmental outcomes are reported in the published literature [see data]. there are dose adjustments for ascorbic acid (vitamin c) use during pregnancy [ see clinical considerations ]. animal reproduction studies have not been conducted with ascor. the estimated background risk of major birth defects and miscarriage for the indicated population is unknown. all pregnancies have a background risk of birth defect, loss, or other adverse outcomes. in the u.s. general population, the estimated background risk of major birth defects and miscarriage in clinically recognized pregnancies is 2-4% and 15-20%, respectively. clinical considerations dose adjustments during pregnancy and post-partum period follow the u.s. recommended dietary allowances (rda) for pregnant women when considering use of ascor for treatment of scurvy [ see dosage and administration (2.3 )]. data human data there are no available data on use of ascor or another ascorbic acid injection in pregnant women. however, a published meta–analysis of randomized studies evaluating a large number of pregnant women who took oral ascorbic acid (vitamin c) (through diet and supplementation) at doses ranging from 500 to1000 mg/day (2.5 to 5 times the recommended daily intravenous dose, respectively) [ see dosage and administration (2.3) ] between the 9th and 16th weeks of pregnancy showed no increased risk of adverse pregnancy outcomes such as miscarriage, preterm premature rupture of membranes, preterm delivery or pregnancy induced hypertension when compared to placebo. these data cannot definitely establish or exclude the absence of a risk with ascorbic acid (vitamin c) during pregnancy. 8.2 lactation risk summary there are no data on the presence of ascorbic acid (vitamin c) in human milk following intravenous dosing in lactating women. ascorbic acid (vitamin c) is present in human milk after maternal oral intake. maternal oral intake of ascorbic acid (vitamin c) exceeding the u.s. recommended dietary allowances (rda) for lactation does not influence the ascorbic acid (vitamin c) content in breast milk or the estimated daily amount received by breastfed infants. there are no data on the effect of ascorbic acid (vitamin c) on milk production or the breastfed infant. the developmental and health benefits of breastfeeding should be considered along with the mother’s clinical need for ascor and any potential adverse effects on the breastfed child from ascor or from the underlying maternal condition. follow the u.s. recommended dietary allowances (rda) for lactating women when considering use of ascor for treatment of scurvy [see dosage and administration (2.3) ]. 8.4 pediatric use ascor is indicated for the short term (up to 1 week) treatment of scurvy in pediatric patients age 5 months and older for whom oral administration is not possible, insufficient or contraindicated. the safety profile of ascorbic acid in pediatric patients is similar to adults; however, pediatric patients less than 2 years of age may be at higher risk of oxalate nephropathy following ascorbic acid administration due to age-related decreased glomerular filtration [ see warnings and precautions (5.1 )]. ascor is not indicated for use in pediatric patients less than 5 months of age. 8.5 geriatric use glomerular filtration rate is known to decrease with age and as such may increase risk for oxalate nephropathy following ascorbic acid administration in elderly population [ see warnings and precautions (5.1 ) ]. 8.6 renal impairment ascor should be used with caution in scorbutic patients with a history of or risk of developing renal oxalate stones or evidence of renal impairment or other issues (e.g., patients on dialysis, patients with diabetic nephropathy, and renal transplant recipients). these patients may be at increased risk of developing acute or chronic oxalate nephropathy following high dose ascorbic acid administration [ see warning and precaution (5.1 ].

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

westminster pharmaceuticals, llc - ascorbic acid (unii: pq6ck8pd0r) (ascorbic acid - unii:pq6ck8pd0r), cholecalciferol (unii: 1c6v77qf41) (cholecalciferol - unii:1c6v77qf41), .alpha.-tocopherol acetate, d- (unii: a7e6112e4n) (.alpha.-tocopherol, d- - unii:n9pr3490h9), thiamine hydrochloride (unii: m572600e5p) (thiamine ion - unii:4abt0j945j), riboflavin (unii: tlm2976ofr) (riboflavin - unii:tlm2976ofr), niacin (unii: 2679mf687a) (niacin - unii:2679mf687a), pyridoxine hydrochloride (unii: 68y4cf58bv) (pyridoxine - unii:kv2jz1bi6z), lev - westgel dha is an orally administered multivitamin/multimineral fatty acid dietary supplement indicated to improve the nutritional status of women throughout pregnancy and in the postnatal period for both lactating and nonlactating mothers. westgel dha can also be beneficial in improving the nutritional status of women prior to conception1. westgel dha is contraindicated in patients with a known hypersensitivity to any of the ingredients. caution is recommended in patients taking anticonvulsant medications as folate may interfere with anticonvulsant medication, and may lower seizure threshold. furthermore, anticonvulsant medications may interfere with folate metabolism.

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u.s. pharmaceutical corporation - ascorbic acid (unii: pq6ck8pd0r) (ascorbic acid - unii:pq6ck8pd0r), cholecalciferol (unii: 1c6v77qf41) (cholecalciferol - unii:1c6v77qf41), thiamine hydrochloride (unii: m572600e5p) (thiamine ion - unii:4abt0j945j), riboflavin (unii: tlm2976ofr) (riboflavin - unii:tlm2976ofr), niacin (unii: 2679mf687a) (niacin - unii:2679mf687a), pyridoxine hydrochloride (unii: 68y4cf58bv) (pyridoxine - unii:kv2jz1bi6z), folic acid (unii: 935e97boy8) (folic acid - unii:935e97boy8), cyanocobalamin (unii: p6yc3eg204) - ascorbic acid 60 mg

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nnodum pharmaceuticals - ferrous fumarate (unii: r5l488ry0q) (ferrous cation - unii:gw89581owr), ascorbic acid (unii: pq6ck8pd0r) (ascorbic acid - unii:pq6ck8pd0r), intrinsic factor (unii: 70bt6oqt2q) (intrinsic factor - unii:70bt6oqt2q), cyanocobalamin (unii: p6yc3eg204) (cyanocobalamin - unii:p6yc3eg204) - ferrous cation 66 mg - for the treatment of all anemias responsive to oral iron therapy, such as hypochromic anemia associated with pregnancy, chronic or acute blood loss, dietary restriction, metabolic disease and post-surgical convalescence. hemochromatosis and hemosiderosis are contraindications to iron therapy.

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

bioactive nutritional, inc. - euphrasia stricta (unii: c9642i91wl) (euphrasia stricta - unii:c9642i91wl), ginkgo (unii: 19fuj2c58t) (ginkgo - unii:19fuj2c58t), petroselinum crispum (unii: 1wza4y92ex) (petroselinum crispum - unii:1wza4y92ex), bilberry (unii: 9p2u39h18w) (bilberry - unii:9p2u39h18w), ascorbic acid (unii: pq6ck8pd0r) (ascorbic acid - unii:pq6ck8pd0r), spigelia anthelmia (unii: wyt05213ge) (spigelia anthelmia - unii:wyt05213ge), sus scrofa eye (unii: x3aok514e6) (sus scrofa eye - unii:x3aok514e6), germanium sesquioxi - euphrasia stricta 3 [hp_x] in 1 ml - for temporary relief of pressure in the eyes, and pain in and around the eyes. for temporary relief of pressure in the eyes, and pain in and around the eyes.