SinuFrin - 13709-231-07 - (Oxymetazoline Hydrochloride)

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Drug Information of SinuFrin

Product NDC: 13709-231
Proprietary Name: SinuFrin
Non Proprietary Name: Oxymetazoline Hydrochloride
Active Ingredient(s): 7.5    mg/15mL & nbsp;   Oxymetazoline Hydrochloride
Administration Route(s): NASAL
Dosage Form(s): SPRAY
Coding System: National Drug Codes(NDC)

Labeler Information of SinuFrin

Product NDC: 13709-231
Labeler Name: NeilMed Pharmaceuticals Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20120715

Package Information of SinuFrin

Package NDC: 13709-231-07
Package Description: 15 mL in 1 BOTTLE (13709-231-07)

NDC Information of SinuFrin

NDC Code 13709-231-07
Proprietary Name SinuFrin
Package Description 15 mL in 1 BOTTLE (13709-231-07)
Product NDC 13709-231
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Oxymetazoline Hydrochloride
Dosage Form Name SPRAY
Route Name NASAL
Start Marketing Date 20120715
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name NeilMed Pharmaceuticals Inc
Substance Name OXYMETAZOLINE HYDROCHLORIDE
Strength Number 7.5
Strength Unit mg/15mL
Pharmaceutical Classes

Complete Information of SinuFrin


General Information