| 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 |