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) |
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 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 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 |