Nasal Decongestant Pe Non Drowsy
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Questions & Answers
Side Effects & Adverse Reactions
Sulfonamides are known to cause Stevens-Johnson syndrome in hypersensitive individuals. Stevens-Johnson syndrome also has been reported following the use of sodium sulfacetamide topically. Cases of drug-induced systemic lupus erythematosus from topical sulfacetamide also have been reported. In one of these cases, there was a fatal outcome. KEEP OUT OF THE REACH OF CHILDREN.
Legal Issues
There is currently no legal information available for this drug.
FDA Safety Alerts
There are currently no FDA safety alerts available for this drug.
Manufacturer Warnings
There is currently no manufacturer warning information available for this drug.
FDA Labeling Changes
There are currently no FDA labeling changes available for this drug.
Uses
This product is intended for topical application in the following scaling dermatoses: seborrheic dermatitis and seborrhea sicca (dandruff). It also is indicated for the treatment of secondary bacterial infections of the skin due to organisms susceptible to sulfonamides.
History
There is currently no drug history available for this drug.
Other Information
Each gram contains 98 mg of sodium sulfacetamide in a vehicle consisting of: benzyl alcohol, cetearyl alcohol (and) PEG-3 distearoylamidoethylmonium methosulfate (and) polysorbate 60, cetyl alcohol, disodium EDTA, fragrance, glyceryl stearate (and) PEG-100 stearate, magnesium aluminum silicate, PEG-150 distearate, phenoxyethanol, polyethylene glycol 400, purified water, sodium lauryl sulfate, sodium thiosulfate, stearyl alcohol and xanthan gum.
Sodium sulfacetamide is a sulfonamide with antibacterial activity. Sodium sulfacetamide is C 8H 9N 2NaO 3S·H 2O with molecular weight of 254.24. Chemically, sodium sulfacetamide is N-[(4-aminophenyl) sulfonyl]-acetamide, monosodium salt, monohydrate. The structural formula is:
Sodium sulfacetamide is an odorless, white, crystalline powder with a bitter taste. It is freely soluble in water, sparingly soluble in alcohol, while practically insoluble in benzene, in chloroform and in ether.
Sources
Nasal Decongestant Pe Non Drowsy Manufacturers
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Cvs Pharmacy
![Nasal Decongestant Pe Non Drowsy (Phenylephrine Hydrochloride) Tablet [Cvs Pharmacy]](/wp-content/themes/bootstrap/assets/img/loading2.gif)
Nasal Decongestant Pe Non Drowsy | Mission Pharmacal Company
Seborrheic dermatitis including seborrhea sicca - Apply to affected areas twice daily (morning and evening), or as directed by your physician. Avoid contact with eyes or mucous membranes. Repeat application as described for eight to ten days. As the condition subsides, the interval between applications may be lengthened. Applications once or twice weekly or every other week may prevent recurrence. Should the condition recur after stopping therapy, the application of this product should be reinitiated as at the beginning of treatment.
Secondary cutaneous bacterial infections - Apply to affected areas twice daily for eight to ten days.
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Hyvee Inc
Nasal Decongestant Pe Non Drowsy | Hyvee Inc
adults and children 12 years and over take 1 tablet every 4 hours do not take more than 6 tablets in 24 hours children under 12 years do not use this product in children under 12 years of age -
Publix Super Markets Inc
Nasal Decongestant Pe Non Drowsy | Publix Super Markets Inc
adults and children 12 years and over
• take 1 tablet every 4 hours • do not take more than 6 tablets in 24 hourschildren under 12 years
do not use this product in children under 12 years of age
![Nasal Decongestant Pe Non Drowsy (Phenylephrine Hydrochloride) Tablet [Hyvee Inc]](http://dailymed.nlm.nih.gov/dailymed/image.cfm?setid=b5dc983c-e27a-48ab-942e-0d5a7a29ccce&name=b5dc983c-e27a-48ab-942e-0d5a7a29ccce-01.jpg)
![Nasal Decongestant Pe Non Drowsy (Phenylephrine Hydrochloride) Tablet [Publix Super Markets Inc]](http://dailymed.nlm.nih.gov/dailymed/image.cfm?setid=3ea6dfa8-9865-4f23-bc9f-101f5f36e0ac&name=ffb0be31-6a30-4cfc-ade4-b328cd12bb9b-01.jpg)
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