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Lantiseptic
Lantiseptic - 12090-0019-1 - (LANOLIN)
Drug Information of Lantiseptic
| Product NDC: | 12090-0019 |
| Proprietary Name: | Lantiseptic |
| Non Proprietary Name: | LANOLIN |
| Active Ingredient(s): | 500 mg/g & nbsp; LANOLIN |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Lantiseptic
| Product NDC: | 12090-0019 |
| Labeler Name: | Summit Industries, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part347 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20091230 |
Package Information of Lantiseptic
| Package NDC: | 12090-0019-1 |
| Package Description: | 14.2 g in 1 JAR (12090-0019-1) |
NDC Information of Lantiseptic
| NDC Code | 12090-0019-1 |
| Proprietary Name | Lantiseptic |
| Package Description | 14.2 g in 1 JAR (12090-0019-1) |
| Product NDC | 12090-0019 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | LANOLIN |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20091230 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Summit Industries, Inc. |
| Substance Name | LANOLIN |
| Strength Number | 500 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
