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benzyl alcohol

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Overview

What is Ulesfia?

      ULESFIA (benzyl alcohol) Lotion is supplied as a white topical lotion containing benzyl alcohol, 5%. Inactive ingredients in this formulation are water, mineral oil, sorbitan monooleate, polysorbate 80, carbomer 934P and trolamine.

      The active ingredient, benzyl alcohol, is a clear, colorless liquid with a mild aromatic odor.  Benzyl alcohol has a molecular mass of 108.14 g/mol. The molecular formula is CHO.

      The chemical structure of benzyl alcohol is:

     

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What does Ulesfia look like?



What are the available doses of Ulesfia?

Lotion, 5% ()

What should I talk to my health care provider before I take Ulesfia?

Pediatric Use: Safety in pediatric patients under six months of age has not been established. ()

How should I use Ulesfia?

      ULESFIA Lotion is indicated for the topical treatment of head lice infestation in patients 6 months of age and older.

     ULESFIA Lotion is not for oral, ophthalmic, or intravaginal use.

     Using the guidelines in Table 1, apply sufficient ULESFIA Lotion to dry hair to completely saturate the scalp and hair; leave on for 10 minutes, then thoroughly rinse off with water. Repeat application after 7 days. Avoid contact with eyes.


What interacts with Ulesfia?

Sorry No Records found


What are the warnings of Ulesfia?

Sorry No Records found


What are the precautions of Ulesfia?

Sorry No Records found


What are the side effects of Ulesfia?

Sorry No records found


What should I look out for while using Ulesfia?

      None.


What might happen if I take too much Ulesfia?

      If oral ingestion occurs, seek medical advice immediately.


How should I store and handle Ulesfia?

StorageStore at 20° to 25°C (68° to 77°F)StorageStore at 20° to 25°C (68° to 77°F)ULESFIA Lotion is a white topical lotion containing benzyl alcohol, 5% (50 mg/g of lotion)       ● NDC 23594-780-08 as an 8 fl oz (227 g) in a polypropylene bottle      ● NDC 23594-780-88 as a package containing two individual 8 fl oz (NDC 23594-780-08) polypropylene bottles with a nit comb      Store at 20º C - 25º C (68º F - 77º F); excursions permitted to 15º C - 30º C (59º F - 86º F) [See USP controlled room temperature].      Do not freeze.ULESFIA Lotion is a white topical lotion containing benzyl alcohol, 5% (50 mg/g of lotion)       ● NDC 23594-780-08 as an 8 fl oz (227 g) in a polypropylene bottle      ● NDC 23594-780-88 as a package containing two individual 8 fl oz (NDC 23594-780-08) polypropylene bottles with a nit comb      Store at 20º C - 25º C (68º F - 77º F); excursions permitted to 15º C - 30º C (59º F - 86º F) [See USP controlled room temperature].      Do not freeze.ULESFIA Lotion is a white topical lotion containing benzyl alcohol, 5% (50 mg/g of lotion)       ● NDC 23594-780-08 as an 8 fl oz (227 g) in a polypropylene bottle      ● NDC 23594-780-88 as a package containing two individual 8 fl oz (NDC 23594-780-08) polypropylene bottles with a nit comb      Store at 20º C - 25º C (68º F - 77º F); excursions permitted to 15º C - 30º C (59º F - 86º F) [See USP controlled room temperature].      Do not freeze.


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Clinical Information

Chemical Structure

No Image found
Clinical Pharmacology

      studies of the effect of ULESFIA Lotion on native, captured lice suggest that benzyl alcohol inhibits lice from closing their respiratory spiracles, allowing the vehicle to obstruct the spiracles and causing the lice to asphyxiate.

     

Non-Clinical Toxicology
      None.

No studies of interactions between Tranexamic acid and other drugs have been conducted.

      Intravenous administration of products containing benzyl alcohol has been associated with neonatal gasping syndrome consisting of severe metabolic acidosis, gasping respirations, progressive hypotension, seizures, central nervous system depression, intraventricular hemorrhage, and death in preterm, low birth weight infants. Neonates (i.e. patients less than 1 month of age or preterm infants with a corrected age of less than 44 weeks) could be at risk for gasping syndrome if treated with ULESFIA Lotion  .  

     

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Reference

This information is obtained from the National Institute of Health's Standard Packaging Label drug database.
"https://dailymed.nlm.nih.gov/dailymed/"

While we update our database periodically, we cannot guarantee it is always updated to the latest version.

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Professional

Clonazepam Description Each single-scored tablet, for oral administration, contains 0.5 mg, 1 mg, or 2 mg Clonazepam, USP, a benzodiazepine. Each tablet also contains corn starch, lactose monohydrate, magnesium stearate, microcrystalline cellulose, and povidone. Clonazepam tablets USP 0.5 mg contain Yellow D&C No. 10 Aluminum Lake. Clonazepam tablets USP 1 mg contain Yellow D&C No. 10 Aluminum Lake, as well as FD&C Blue No. 1 Aluminum Lake. Chemically, Clonazepam, USP is 5-(o-chlorophenyl)-1,3-dihydro-7-nitro-2H-1,4-benzodiazepin-2-one. It is a light yellow crystalline powder. It has the following structural formula: C15H10ClN3O3 M.W. 315.72
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Interactions

Interactions

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