| Product NDC: | 51346-218 |
| Proprietary Name: | ORIGINAL POWER REFIRMING AMPOULE |
| Non Proprietary Name: | Allantoin |
| Active Ingredient(s): | .6 mg/30mL & nbsp; Allantoin |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 51346-218 |
| Labeler Name: | NATURE REPUBLIC CO., LTD. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part347 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20130201 |
| Package NDC: | 51346-218-01 |
| Package Description: | 30 mL in 1 CARTON (51346-218-01) |
| NDC Code | 51346-218-01 |
| Proprietary Name | ORIGINAL POWER REFIRMING AMPOULE |
| Package Description | 30 mL in 1 CARTON (51346-218-01) |
| Product NDC | 51346-218 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Allantoin |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20130201 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | NATURE REPUBLIC CO., LTD. |
| Substance Name | ALLANTOIN |
| Strength Number | .6 |
| Strength Unit | mg/30mL |
| Pharmaceutical Classes |