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PLACENTA EX DAY
PLACENTA EX DAY - 51346-029-01 - (OCTINOXATE)
Drug Information of PLACENTA EX DAY
| Product NDC: | 51346-029 |
| Proprietary Name: | PLACENTA EX DAY |
| Non Proprietary Name: | OCTINOXATE |
| Active Ingredient(s): | 3.75 g/50mL & nbsp; OCTINOXATE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of PLACENTA EX DAY
| Product NDC: | 51346-029 |
| Labeler Name: | NATURE REPUBLIC CO., LTD. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120301 |
Package Information of PLACENTA EX DAY
| Package NDC: | 51346-029-01 |
| Package Description: | 50 mL in 1 CARTON (51346-029-01) |
NDC Information of PLACENTA EX DAY
| NDC Code | 51346-029-01 |
| Proprietary Name | PLACENTA EX DAY |
| Package Description | 50 mL in 1 CARTON (51346-029-01) |
| Product NDC | 51346-029 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20120301 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | NATURE REPUBLIC CO., LTD. |
| Substance Name | OCTINOXATE |
| Strength Number | 3.75 |
| Strength Unit | g/50mL |
| Pharmaceutical Classes |
