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Sooryehan Pure-Whitening Essence
Sooryehan Pure-Whitening Essence - 53208-442-02 - (POLYDATIN)
Drug Information of Sooryehan Pure-Whitening Essence
| Product NDC: | 53208-442 |
| Proprietary Name: | Sooryehan Pure-Whitening Essence |
| Non Proprietary Name: | POLYDATIN |
| Active Ingredient(s): | .22 1/100mL & nbsp; POLYDATIN |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sooryehan Pure-Whitening Essence
| Product NDC: | 53208-442 |
| Labeler Name: | LG Household and Healthcare, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20100514 |
Package Information of Sooryehan Pure-Whitening Essence
| Package NDC: | 53208-442-02 |
| Package Description: | 1 CONTAINER in 1 BOX (53208-442-02) > 45 mL in 1 CONTAINER (53208-442-01) |
NDC Information of Sooryehan Pure-Whitening Essence
| NDC Code | 53208-442-02 |
| Proprietary Name | Sooryehan Pure-Whitening Essence |
| Package Description | 1 CONTAINER in 1 BOX (53208-442-02) > 45 mL in 1 CONTAINER (53208-442-01) |
| Product NDC | 53208-442 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | POLYDATIN |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20100514 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | LG Household and Healthcare, Inc. |
| Substance Name | POLYDATIN |
| Strength Number | .22 |
| Strength Unit | 1/100mL |
| Pharmaceutical Classes |
