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JOURNEE
JOURNEE - 52318-002-03 - (OCTINOXATE, ZINC OXIDE)
Drug Information of JOURNEE
| Product NDC: | 52318-002 |
| Proprietary Name: | JOURNEE |
| Non Proprietary Name: | OCTINOXATE, ZINC OXIDE |
| Active Ingredient(s): | 75; 73 mg/mL; mg/mL & nbsp; OCTINOXATE, ZINC OXIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of JOURNEE
| Product NDC: | 52318-002 |
| Labeler Name: | Neocutis, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20120618 |
Package Information of JOURNEE
| Package NDC: | 52318-002-03 |
| Package Description: | 200 mL in 1 BOTTLE (52318-002-03) |
NDC Information of JOURNEE
| NDC Code | 52318-002-03 |
| Proprietary Name | JOURNEE |
| Package Description | 200 mL in 1 BOTTLE (52318-002-03) |
| Product NDC | 52318-002 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE, ZINC OXIDE |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20120618 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Neocutis, Inc. |
| Substance Name | OCTINOXATE; ZINC OXIDE |
| Strength Number | 75; 73 |
| Strength Unit | mg/mL; mg/mL |
| Pharmaceutical Classes |
