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Zippity Doos
Zippity Doos - 57240-2027-1 - (Rosemary)
Drug Information of Zippity Doos
| Product NDC: | 57240-2027 |
| Proprietary Name: | Zippity Doos |
| Non Proprietary Name: | Rosemary |
| Active Ingredient(s): | .023 mg/mL & nbsp; Rosemary |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Zippity Doos
| Product NDC: | 57240-2027 |
| Labeler Name: | Laurus Enterprises, LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 20100301 |
Package Information of Zippity Doos
| Package NDC: | 57240-2027-1 |
| Package Description: | 245 mL in 1 BOTTLE (57240-2027-1) |
NDC Information of Zippity Doos
| NDC Code | 57240-2027-1 |
| Proprietary Name | Zippity Doos |
| Package Description | 245 mL in 1 BOTTLE (57240-2027-1) |
| Product NDC | 57240-2027 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Rosemary |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20100301 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | Laurus Enterprises, LLC |
| Substance Name | ROSEMARY |
| Strength Number | .023 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
