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OB Towelette
OB Towelette - 50730-5102-0 - (benzalkonium chloride)
Drug Information of OB Towelette
| Product NDC: | 50730-5102 |
| Proprietary Name: | OB Towelette |
| Non Proprietary Name: | benzalkonium chloride |
| Active Ingredient(s): | .004 mL/1 & nbsp; benzalkonium chloride |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of OB Towelette
| Product NDC: | 50730-5102 |
| Labeler Name: | H and P Industries, Inc. dba Triad Group |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333A |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 19990701 |
Package Information of OB Towelette
| Package NDC: | 50730-5102-0 |
| Package Description: | 100 POUCH in 1 CARTON (50730-5102-0) > 1 SOLUTION in 1 POUCH |
NDC Information of OB Towelette
| NDC Code | 50730-5102-0 |
| Proprietary Name | OB Towelette |
| Package Description | 100 POUCH in 1 CARTON (50730-5102-0) > 1 SOLUTION in 1 POUCH |
| Product NDC | 50730-5102 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | benzalkonium chloride |
| Dosage Form Name | SOLUTION |
| Route Name | TOPICAL |
| Start Marketing Date | 19990701 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | H and P Industries, Inc. dba Triad Group |
| Substance Name | BENZALKONIUM CHLORIDE |
| Strength Number | .004 |
| Strength Unit | mL/1 |
| Pharmaceutical Classes |
