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CVS Pharmacy - 48871-000-00 - (benzalkonium chloride, pramoxine hydrochloride)

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Drug Information of CVS Pharmacy

Product NDC: 48871-000
Proprietary Name: CVS Pharmacy
Non Proprietary Name: benzalkonium chloride, pramoxine hydrochloride
Active Ingredient(s): .195; .15    mL/15mL; mL/15mL & nbsp;   benzalkonium chloride, pramoxine hydrochloride
Administration Route(s): TOPICAL
Dosage Form(s): SPRAY
Coding System: National Drug Codes(NDC)

Labeler Information of CVS Pharmacy

Product NDC: 48871-000
Labeler Name: Health-Tech, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part310.545
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20100119

Package Information of CVS Pharmacy

Package NDC: 48871-000-00
Package Description: 12 CARTON in 1 BOX (48871-000-00) > 6 BLISTER PACK in 1 CARTON > 1 BOTTLE, SPRAY in 1 BLISTER PACK > 15 mL in 1 BOTTLE, SPRAY

NDC Information of CVS Pharmacy

NDC Code 48871-000-00
Proprietary Name CVS Pharmacy
Package Description 12 CARTON in 1 BOX (48871-000-00) > 6 BLISTER PACK in 1 CARTON > 1 BOTTLE, SPRAY in 1 BLISTER PACK > 15 mL in 1 BOTTLE, SPRAY
Product NDC 48871-000
Product Type Name HUMAN OTC DRUG
Non Proprietary Name benzalkonium chloride, pramoxine hydrochloride
Dosage Form Name SPRAY
Route Name TOPICAL
Start Marketing Date 20100119
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Health-Tech, Inc.
Substance Name BENZALKONIUM CHLORIDE; PRAMOXINE HYDROCHLORIDE
Strength Number .195; .15
Strength Unit mL/15mL; mL/15mL
Pharmaceutical Classes

Complete Information of CVS Pharmacy


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