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AMOREPACIFIC
AMOREPACIFIC - 43419-501-01 - (OCTINOXATE and TITANIUM DIOXIDE)
Drug Information of AMOREPACIFIC
| Product NDC: | 43419-501 |
| Proprietary Name: | AMOREPACIFIC |
| Non Proprietary Name: | OCTINOXATE and TITANIUM DIOXIDE |
| Active Ingredient(s): | 2.5; 1.05 mL/50mL; mL/50mL & nbsp; OCTINOXATE and TITANIUM DIOXIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of AMOREPACIFIC
| Product NDC: | 43419-501 |
| Labeler Name: | AMOREPACIFIC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110601 |
Package Information of AMOREPACIFIC
| Package NDC: | 43419-501-01 |
| Package Description: | 50 mL in 1 TUBE (43419-501-01) |
NDC Information of AMOREPACIFIC
| NDC Code | 43419-501-01 |
| Proprietary Name | AMOREPACIFIC |
| Package Description | 50 mL in 1 TUBE (43419-501-01) |
| Product NDC | 43419-501 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE and TITANIUM DIOXIDE |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20110601 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | AMOREPACIFIC |
| Substance Name | OCTINOXATE; TITANIUM DIOXIDE |
| Strength Number | 2.5; 1.05 |
| Strength Unit | mL/50mL; mL/50mL |
| Pharmaceutical Classes |
