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

zhejiang yongtai pharmaceutical co., ltd. - gabapentin (unii: 6cw7f3g59x) (gabapentin - unii:6cw7f3g59x) - gabapentin is indicated for: - management of postherpetic neuralgia in adults - adjunctive therapy in the treatment of partial onset seizures, with and without secondary generalization, in adults and pediatric patients 3 years and older with epilepsy gabapentin is contraindicated in patients who have demonstrated hypersensitivity to the drug or its ingredients. pregnancy exposure registry there is a pregnancy exposure registry that monitors pregnancy outcomes in women exposed to antiepileptic drugs (aeds), such as gabapentin, during pregnancy. encourage women who are taking gabapentin during pregnancy to enroll in the north american antiepileptic drug (naaed) pregnancy registry by calling the toll free number 1-888-233-2334 or visiting http://www.aedpregnancyregistry.org/ . risk summary there are no adequate data on the developmental risks associated with the use of gabapentin in pregnant women. in nonclinical studies in mice, rats, and rabbits, gabapentin was developmentally toxic (increased fetal skeletal a

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

zhejiang dingtai pharmaceutical co.; ltd - menthol   0.5%, methyl salicylate  0.5% - menthol   external analgesic methyl salicylate     external analgesic for the temporary relief of minor aches and pains of muscles and joints due to: simple backache arthritis strains bruises sprains on wounds on irritated or damaged skin if the appearance of this product has changed in excess of 12 hours if you have known hypersensitive to this product otherwise than as directed pregnant taking other medications condition worsens symptoms persist for more than 7 days symptoms clear up and occur again within a few days excessive irritation of the skin develops when using for pain of arthritis pain persists for more than 10 days redness is present in conditions affecting children under 12 years of age

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

zhejiang dingtai pharmaceutical co., ltd - camphor (synthetic) (unii: 5tjd82a1et) (camphor (synthetic) - unii:5tjd82a1et), menthol (unii: l7t10eip3a) (menthol - unii:l7t10eip3a) - purpose external analgesic external analgesic uses for the temporary relief of minor aches and pains of muscles and joints due to: ■ simple backache ■ arthritis ■ strains ■ bruises ■ sprains do not use ■ on irritated or damaged skin ■ on wounds stop use and ask a doctor if ■ condition worsens ■ symptoms persist for more than 7 days ■ symptoms clear up and occur again within a few days ■ excessive irritation of the skin develops ■ nausea, vomiting, abdominal discomfort, diarrhea, or skin rash occurs ■ you feel actual pain or experience blistering or burning after application (it is normal to feel a warming or cooling sensation) ■ when using for pain of arthritis:       ■ pain persists for more than 10 days ■ redness is present       ■ in conditions affecting children under 12 years of age

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

zhejiang dingtai pharmaceutical co., ltd - salicylic acid (unii: o414pz4lpz) (salicylic acid - unii:o414pz4lpz) - purpose corn and callus remover uses for the removal of corns and calluses relieves pain by removing corns and calluses do not use on irritated skin on any area that is infected or reddened if you are a diabetic if you have poor blood circulation

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

zhejiang dingtai pharmaceutical co., ltd - camphor (synthetic) (unii: 5tjd82a1et) (camphor (synthetic) - unii:5tjd82a1et), menthol (unii: l7t10eip3a) (menthol - unii:l7t10eip3a) - purpose external analgesic external analgesic uses for the temporary relief of minor aches and pains of muscles and joints due to: ■ simple backache ■ arthritis ■ strains ■ bruises ■ sprains do not use 
■ on irritated or damaged skin ■ on wounds
 ■ if you are allergic to any ingredient in this product stop use and ask a doctor if ■ condition worsens
 ■ symptoms persist for more than 7 days
 ■ symptoms clear up and occur again within a few days ■ excessive irritation of the skin develops 
■ nausea, vomiting, abdominal discomfort, diarrhea, or skin rash occurs ■ you feel actual pain or experience blistering or burning after application (it is normal to feel a warming or cooling sensation) ■ when using for pain of arthritis:    ■ pain persists for more than 10 days    ■ redness is present    ■ in conditions affecting children under 12 years of age

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

zhejiang dingtai pharmaceutical co., ltd - tolnaftate (unii: 06kb629tkv) (tolnaftate - unii:06kb629tkv) - purpose antifungal uses proven clinically effective in the treatment of most athlete’s foot (tinea pedis) and ringworm (tinea corporis) helps prevent most athlete’s foot with daily use
for effective relief of itching, burning, and cracking do not use
 on children under 2 years of age unless directed by a doctor stop use and ask a doctor if
 irritation occurs
 there is no improvement within 4 weeks

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

zhejiang dingtai pharmaceutical co., ltd - miconazole nitrate (unii: vw4h1cyw1k) (miconazole - unii:7nno0d7s5m) - purpose antifungal uses cures most jock itch (tinea cruris)
 relieves the following symptoms associated with jock itch:    itching    scaling    cracking    burning    discomfort    soreness    irritation    redness do not use
 on children under 2 years of age unless directed by a doctor stop use and ask a doctor if
 irritation occurs 
there is no improvement within 2 weeks

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

zhejiang dingtai pharmaceutical co., ltd - clotrimazole (unii: g07gz97h65) (clotrimazole - unii:g07gz97h65) - purpose antifungal uses cures most ringworm (tinea corporis) relieves    itching    scaling    cracking    burning    discomfort    soreness    irritation    redness do not use on children under 2 years of age unless directed by a doctor stop use and ask a doctor if 
irritation occurs 
there is no improvement within 4 weeks

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

zhejiang dingtai pharmaceutical co., ltd - zinc oxide (unii: soi2loh54z) (zinc cation - unii:13s1s8sf37), ferric oxide red (unii: 1k09f3g675) (ferric oxide red - unii:1k09f3g675), diphenhydramine hydrochloride (unii: tc2d6jad40) (diphenhydramine - unii:8gts82s83m) - purpose skin protectant external analgesic uses for the temporary relief of pain, itching, and rushes due to: poison ivy poison oak poison sumac dries the oozing and weeping of: poison ivy poison oak poison sumac stop use and ask a doctor if
 conditions worsens condition does not improve within 7 days symptoms clear up and occur again within a few days

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

preferred pharmaceuticals inc. - paroxetine hydrochloride anhydrous (unii: 3i3t11ud2s) (paroxetine - unii:41vrh5220h) - paroxetine 20 mg - major depressive disorder: paroxetine tablets are indicated for the treatment of major depressive disorder. the efficacy of paroxetine tablets in the treatment of a major depressive episode was established in 6-week controlled trials of outpatients whose diagnoses corresponded most closely to the dsm-iii category of major depressive disorder (see clinical pharmacology: clinical trials ). a major depressive episode implies a prominent and relatively persistent depressed or dysphoric mood that usually interferes with daily functioning (nearly every day for at least 2 weeks); it should include at least 4 of the following 8 symptoms: change in appetite, change in sleep, psychomotor agitation or retardation, loss of interest in usual activities or decrease in sexual drive, increased fatigue, feelings of guilt or worthlessness, slowed thinking or impaired concentration, and a suicide attempt or suicidal ideation. the effects of paroxetine tablets in hospitalized depressed patients have not been adequately studied.