Home
>
National Drug Code (NDC)
>
O HUI WHITE EXTREME CELLIGHT
O HUI WHITE EXTREME CELLIGHT - 53208-501-02 - (PROTOCATECHUALDEHYDE)
Drug Information of O HUI WHITE EXTREME CELLIGHT
| Product NDC: | 53208-501 |
| Proprietary Name: | O HUI WHITE EXTREME CELLIGHT |
| Non Proprietary Name: | PROTOCATECHUALDEHYDE |
| Active Ingredient(s): | .0315 mL/100mL & nbsp; PROTOCATECHUALDEHYDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | EMULSION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of O HUI WHITE EXTREME CELLIGHT
| Product NDC: | 53208-501 |
| Labeler Name: | LG Household and Healthcare, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20110307 |
Package Information of O HUI WHITE EXTREME CELLIGHT
| Package NDC: | 53208-501-02 |
| Package Description: | 1 CONTAINER in 1 BOX (53208-501-02) > 150 mL in 1 CONTAINER (53208-501-01) |
NDC Information of O HUI WHITE EXTREME CELLIGHT
| NDC Code | 53208-501-02 |
| Proprietary Name | O HUI WHITE EXTREME CELLIGHT |
| Package Description | 1 CONTAINER in 1 BOX (53208-501-02) > 150 mL in 1 CONTAINER (53208-501-01) |
| Product NDC | 53208-501 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | PROTOCATECHUALDEHYDE |
| Dosage Form Name | EMULSION |
| Route Name | TOPICAL |
| Start Marketing Date | 20110307 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | LG Household and Healthcare, Inc. |
| Substance Name | PROTOCATECHUALDEHYDE |
| Strength Number | .0315 |
| Strength Unit | mL/100mL |
| Pharmaceutical Classes |
