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ISAKNOX WHITE SYMPHONY BRIGHTENING EMULSION
ISAKNOX WHITE SYMPHONY BRIGHTENING EMULSION - 53208-385-02 - (ARBUTIN)
Drug Information of ISAKNOX WHITE SYMPHONY BRIGHTENING EMULSION
| Product NDC: | 53208-385 |
| Proprietary Name: | ISAKNOX WHITE SYMPHONY BRIGHTENING EMULSION |
| Non Proprietary Name: | ARBUTIN |
| Active Ingredient(s): | 2.1 g/100g & nbsp; ARBUTIN |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ISAKNOX WHITE SYMPHONY BRIGHTENING EMULSION
| Product NDC: | 53208-385 |
| Labeler Name: | LG Household and Healthcare, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part358 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20100329 |
Package Information of ISAKNOX WHITE SYMPHONY BRIGHTENING EMULSION
| Package NDC: | 53208-385-02 |
| Package Description: | 1 CONTAINER in 1 BOX (53208-385-02) > 120 g in 1 CONTAINER (53208-385-01) |
NDC Information of ISAKNOX WHITE SYMPHONY BRIGHTENING EMULSION
| NDC Code | 53208-385-02 |
| Proprietary Name | ISAKNOX WHITE SYMPHONY BRIGHTENING EMULSION |
| Package Description | 1 CONTAINER in 1 BOX (53208-385-02) > 120 g in 1 CONTAINER (53208-385-01) |
| Product NDC | 53208-385 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ARBUTIN |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20100329 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | LG Household and Healthcare, Inc. |
| Substance Name | ARBUTIN |
| Strength Number | 2.1 |
| Strength Unit | g/100g |
| Pharmaceutical Classes |
