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rx act nasal - 37808-817-10 - (oxymetazoline hydrochloride)

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Drug Information of rx act nasal

Product NDC: 37808-817
Proprietary Name: rx act nasal
Non Proprietary Name: oxymetazoline hydrochloride
Active Ingredient(s): .05    g/100mL & nbsp;   oxymetazoline hydrochloride
Administration Route(s): NASAL
Dosage Form(s): SPRAY
Coding System: National Drug Codes(NDC)

Labeler Information of rx act nasal

Product NDC: 37808-817
Labeler Name: H E B
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20000825

Package Information of rx act nasal

Package NDC: 37808-817-10
Package Description: 1 BOTTLE, SPRAY in 1 CARTON (37808-817-10) > 30 mL in 1 BOTTLE, SPRAY

NDC Information of rx act nasal

NDC Code 37808-817-10
Proprietary Name rx act nasal
Package Description 1 BOTTLE, SPRAY in 1 CARTON (37808-817-10) > 30 mL in 1 BOTTLE, SPRAY
Product NDC 37808-817
Product Type Name HUMAN OTC DRUG
Non Proprietary Name oxymetazoline hydrochloride
Dosage Form Name SPRAY
Route Name NASAL
Start Marketing Date 20000825
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name H E B
Substance Name OXYMETAZOLINE HYDROCHLORIDE
Strength Number .05
Strength Unit g/100mL
Pharmaceutical Classes

Complete Information of rx act nasal


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