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Lavender Foaming
Lavender Foaming - 66949-834-01 - (Triclosan)
Drug Information of Lavender Foaming
| Product NDC: | 66949-834 |
| Proprietary Name: | Lavender Foaming |
| Non Proprietary Name: | Triclosan |
| Active Ingredient(s): | .01 g/10mL & nbsp; Triclosan |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Lavender Foaming
| Product NDC: | 66949-834 |
| Labeler Name: | Zep Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333A |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20071010 |
Package Information of Lavender Foaming
| Package NDC: | 66949-834-01 |
| Package Description: | 1000 mL in 1 BOTTLE, PLASTIC (66949-834-01) |
NDC Information of Lavender Foaming
| NDC Code | 66949-834-01 |
| Proprietary Name | Lavender Foaming |
| Package Description | 1000 mL in 1 BOTTLE, PLASTIC (66949-834-01) |
| Product NDC | 66949-834 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Triclosan |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20071010 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Zep Inc. |
| Substance Name | TRICLOSAN |
| Strength Number | .01 |
| Strength Unit | g/10mL |
| Pharmaceutical Classes |
