| Product NDC: | 65923-007 |
| Proprietary Name: | FAMILY CARE TRIPLE ANTIBIOTIC PAIN RELIEF |
| Non Proprietary Name: | NEOMYCIN SULFATE |
| Active Ingredient(s): | 3.5 mg/g & nbsp; NEOMYCIN SULFATE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 65923-007 |
| Labeler Name: | UNITED EXCHANGE CORP. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333B |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120207 |
| Package NDC: | 65923-007-23 |
| Package Description: | 1 TUBE in 1 CARTON (65923-007-23) > 28 g in 1 TUBE |
| NDC Code | 65923-007-23 |
| Proprietary Name | FAMILY CARE TRIPLE ANTIBIOTIC PAIN RELIEF |
| Package Description | 1 TUBE in 1 CARTON (65923-007-23) > 28 g in 1 TUBE |
| Product NDC | 65923-007 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | NEOMYCIN SULFATE |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 20120207 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | UNITED EXCHANGE CORP. |
| Substance Name | NEOMYCIN SULFATE |
| Strength Number | 3.5 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |