| 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 |