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THE QUEEN ROSE
THE QUEEN ROSE - 55885-010-01 - (WITCH HAZEL)
Drug Information of THE QUEEN ROSE
| Product NDC: | 55885-010 |
| Proprietary Name: | THE QUEEN ROSE |
| Non Proprietary Name: | WITCH HAZEL |
| Active Ingredient(s): | .005 mg/5mL & nbsp; WITCH HAZEL |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of THE QUEEN ROSE
| Product NDC: | 55885-010 |
| Labeler Name: | LaLa Co., Ltd. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part347 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20121201 |
Package Information of THE QUEEN ROSE
| Package NDC: | 55885-010-01 |
| Package Description: | 5 mL in 1 CARTON (55885-010-01) |
NDC Information of THE QUEEN ROSE
| NDC Code | 55885-010-01 |
| Proprietary Name | THE QUEEN ROSE |
| Package Description | 5 mL in 1 CARTON (55885-010-01) |
| Product NDC | 55885-010 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | WITCH HAZEL |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20121201 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | LaLa Co., Ltd. |
| Substance Name | WITCH HAZEL |
| Strength Number | .005 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes |
