Product NDC: | 0280-0730 |
Proprietary Name: | Bactine Pain Relieving |
Non Proprietary Name: | BENZALKONIUM CHLORIDE and LIDOCAINE HYDROCHLORIDE |
Active Ingredient(s): | .13; 2.5 g/100mL; g/100mL & nbsp; BENZALKONIUM CHLORIDE and LIDOCAINE HYDROCHLORIDE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0280-0730 |
Labeler Name: | Bayer HealthCare LLC, Consumer Care |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333A |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20020924 |
Package NDC: | 0280-0730-05 |
Package Description: | 150 mL in 1 BOTTLE, SPRAY (0280-0730-05) |
NDC Code | 0280-0730-05 |
Proprietary Name | Bactine Pain Relieving |
Package Description | 150 mL in 1 BOTTLE, SPRAY (0280-0730-05) |
Product NDC | 0280-0730 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | BENZALKONIUM CHLORIDE and LIDOCAINE HYDROCHLORIDE |
Dosage Form Name | LIQUID |
Route Name | TOPICAL |
Start Marketing Date | 20020924 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Bayer HealthCare LLC, Consumer Care |
Substance Name | BENZALKONIUM CHLORIDE; LIDOCAINE HYDROCHLORIDE |
Strength Number | .13; 2.5 |
Strength Unit | g/100mL; g/100mL |
Pharmaceutical Classes |