DOXYCYCLINE HYCLATE capsule, gelatin coated USA - engelsk - NLM (National Library of Medicine)

doxycycline hyclate capsule, gelatin coated

pd-rx pharmaceuticals, inc. - doxycycline hyclate (unii: 19xts3t51u) (doxycycline anhydrous - unii:334895s862) - to reduce the development of drug-resistant bacteria and maintain effectiveness of doxycycline hyclate capsules and other antibacterial drugs, doxycycline hyclate capsules should be used only to treat or prevent infections that are proven or strongly suspected to be caused by susceptible bacteria. when culture and susceptibility information are available, they should be considered in selecting or modifying antibacterial therapy. in the absence of such data, local epidemiology and susceptibility patterns may contribute to the empiric selection of therapy. doxycycline is indicated for the treatment of the following infections: - rocky mountain spotted fever, typhus fever and the typhus group, q fever, rickettsialpox, and tick fevers caused by rickettsiae. - respiratory tract infections caused by mycoplasma pneumoniae . - lymphogranuloma venereum caused by chlamydia trachomatis . - psittacosis (ornithosis) caused by chlamydophila psittaci . - trachoma caused

ACETAMINOPHEN AND CODEINE PHOSPHATE tablet USA - engelsk - NLM (National Library of Medicine)

acetaminophen and codeine phosphate tablet

proficient rx lp - acetaminophen (unii: 362o9itl9d) (acetaminophen - unii:362o9itl9d), codeine phosphate (unii: gsl05y1mn6) (codeine anhydrous - unii:ux6owy2v7j) - acetaminophen and codeine phosphate tablets are indicated for the relief of mild to moderately severe pain. codeine-containing products are contraindicated for postoperative pain management in children who have undergone tonsillectomy and/or adenoidectomy. this product should not be administered to patients who have previously exhibited hypersensitivity to codeine or acetaminophen.  controlled substance acetaminophen and codeine phosphate tablets are classified as a schedule iii controlled substance. abuse and dependence codeine can produce drug dependence of the morphine type and, therefore, has the potential for being abused. psychological dependence, physical dependence, and tolerance may develop upon repeated administration and it should be prescribed and administered with the same degree of caution appropriate to the use of other oral narcotic medications.

METHYLPREDNISOLONE tablet USA - engelsk - NLM (National Library of Medicine)

methylprednisolone tablet

tianjin tianyao pharmaceuticals co., ltd. - methylprednisolone (unii: x4w7zr7023) (methylprednisolone - unii:x4w7zr7023) - methylprednisolone tablets are indicated in the following conditions: 1. endocrine disorders primary or secondary adrenocortical insufficiency (hydrocortisone or cortisone is the first choice; synthetic analogs may be used in conjunction with mineralocorticoids where applicable; in infancy mineralocorticoid supplementation is of particular importance). congenital adrenal hyperplasia nonsuppurative thyroiditis hypercalcemia associated with cancer 2. rheumatic disorders as adjunctive therapy for short-term administration (to tide the patient over an acute episode or exacerbation) in: rheumatoid arthritis, including juvenile rheumatoid arthritis (selected cases may require low-dose maintenance therapy) ankylosing spondylitis acute and subacute bursitis synovitis of osteoarthritis acute nonspecific tenosynovitis post-traumatic osteoarthritis psoriatic arthritis epicondylitis acute gouty arthritis 3. collagen diseases during an exacerbation or as maintenance therapy in selected cases of: systemic lupus erythematos

MAXIMUM STRENGTH PAIN CREAM WITH PURE HEMP EXTRACT- pain cream cream USA - engelsk - NLM (National Library of Medicine)

maximum strength pain cream with pure hemp extract- pain cream cream

royal labs natural cosmetics - menthol 10%, methyl salicylate 10%, camphor bark oil 3%, eucalyptus leaf oil 2% - directions: adults and children 12 years of age and older: rub onto affected area 3 to 4 times daily; children under 12 years of age ask a doctor. uses: for temporary relief of minor aches and pains of muscles and joints associated with: arthritis, muscle strain, bruises, sprains, backache

DOC BLOCK BODY ESSENTIAL SUNSCREEN BROAD SPECTRUM SPF30- sunscreen lotion USA - engelsk - NLM (National Library of Medicine)

doc block body essential sunscreen broad spectrum spf30- sunscreen lotion

garth fisher beauty llc - avobenzone 3.0%, homosalate 8.0%, octisalate 5.0%, octocrylene 4.0%, oxybenzone 4.0% - sunscreen - helps prevent sunburn - higher spf gives more sunburn protection

XCEPTOR CBD PAIN MENTHOL- methyl salicylate cream USA - engelsk - NLM (National Library of Medicine)

xceptor cbd pain menthol- methyl salicylate cream

xceptor llc - methyl salicylate  10% - topical analgesic topical pain relief for minor aches and pains.

ROCKSAUCE FIRE- methyl salicylate, menthol and capsaicin cream USA - engelsk - NLM (National Library of Medicine)

rocksauce fire- methyl salicylate, menthol and capsaicin cream

ningbo sante ying medicaland healthdevelopment co.,ltd - methyl salicylate 20%, menthol usp 10%, capsaicin 0.002% - topical analgesic for temporary relief minor muscular discomfort if conditions persist for more than 1 week or reocur.

NU-DERM SYSTEM NORMAL-DRY SKIN TRANSFORMATION- hydroquinone, octisalate and zinc oxide kit USA - engelsk - NLM (National Library of Medicine)

nu-derm system normal-dry skin transformation- hydroquinone, octisalate and zinc oxide kit

obagi cosmeceutical llc - hydroquinone (unii: xv74c1n1ae) (hydroquinone - unii:xv74c1n1ae) - for the gradual bleaching of hyperpigmented skin conditions such as chloasma, melasma, freckles, senile lentigines and other unwanted areas of melanin hyperpigmentation. people with prior history of sensitivity or allergic reaction to this product or any of its ingredients should not use it. the safety of topical hydroquinone use during pregnancy or in children (12 years and under) has not been established. - helps prevent sunburn - if used as directed with other sun protection measures (see directions ), decreases the risk of skin cancer and early skin aging caused by the sun

BLACKMONSTER DAY AND NIGHT MOISTURIZER- sunscreen cream USA - engelsk - NLM (National Library of Medicine)

blackmonster day and night moisturizer- sunscreen cream

blank corporation - octinoxate (unii: 4y5p7mud51) (octinoxate - unii:4y5p7mud51), octisalate (unii: 4x49y0596w) (octisalate - unii:4x49y0596w), octocrylene (unii: 5a68wgf6wm) (octocrylene - unii:5a68wgf6wm), ensulizole (unii: 9yq9di1w42) (ensulizole - unii:9yq9di1w42), titanium dioxide (unii: 15fix9v2jp) (titanium dioxide - unii:15fix9v2jp) - sunscreen ■ helps prevent sunburn. ■ if used as directed with other sun protection measures (see directions), decreases the risk of skin cancer and early skin aging caused by the sun. ■ apply liberally 15 minutes before sun exposure. ■ reapply at least every 2 hours. ■ use a waterresistant sunscreen if swimming or sweating. ■ sun protection measures. spending time in the sun increases your risk of skin cancer and early skin aging. to decrease this risk, regularly use a sunscreen with a broad spectrum spf value of 15 or higher and other sun protection measures including: ■ limit time in the sun, especially from 10 a.m. - 2 p.m. ■ wear long-sleeved shirts, pants, hats, and sunglasses. ■ children under 6 months of age: ask a doctor

ACETAMINOPHEN AND CODEINE tablet USA - engelsk - NLM (National Library of Medicine)

acetaminophen and codeine tablet

asclemed usa, inc. - acetaminophen (unii: 362o9itl9d) (acetaminophen - unii:362o9itl9d), codeine phosphate (unii: gsl05y1mn6) (codeine anhydrous - unii:ux6owy2v7j) - acetaminophen and codeine phosphate tablets are indicated for the management of mild to moderate pain, where treatment with an opioid is appropriate and for which alternative treatments are inadequate. limitations of use because of the risks of addiction, abuse, and misuse, with opioids, even at recommended doses (see warnings ), reserve acetaminophen and codeine phosphate tablets for use in patients for whom alternative treatment options (e.g., non-opioid analgesics). - have not provided adequate analgesia, or are not expected to provide adequate analgesia, have not provided adequate analgesia, or are not expected to provide adequate analgesia, - have not been tolerated, or are not expected to be tolerated. have not been tolerated, or are not expected to be tolerated. acetaminophen and codeine phosphate tablets are contraindicated for: - all children younger than 12 years of age (see warnings ). all children younger than 12 years of age (see warnings )