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ISA KNOX 365 SUN
ISA KNOX 365 SUN - 53208-502-02 - (ZINC OXIDE, TITANIUM DIOXIDE, OCTINOXATE)
Drug Information of ISA KNOX 365 SUN
| Product NDC: | 53208-502 |
| Proprietary Name: | ISA KNOX 365 SUN |
| Non Proprietary Name: | ZINC OXIDE, TITANIUM DIOXIDE, OCTINOXATE |
| Active Ingredient(s): | 7.2; 4.03; 11.04 mL/100mL; mL/100mL; mL/100mL & nbsp; ZINC OXIDE, TITANIUM DIOXIDE, OCTINOXATE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ISA KNOX 365 SUN
| Product NDC: | 53208-502 |
| Labeler Name: | LG Household and Healthcare, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20100330 |
Package Information of ISA KNOX 365 SUN
| Package NDC: | 53208-502-02 |
| Package Description: | 1 CONTAINER in 1 BOX (53208-502-02) > 70 mL in 1 CONTAINER (53208-502-01) |
NDC Information of ISA KNOX 365 SUN
| NDC Code | 53208-502-02 |
| Proprietary Name | ISA KNOX 365 SUN |
| Package Description | 1 CONTAINER in 1 BOX (53208-502-02) > 70 mL in 1 CONTAINER (53208-502-01) |
| Product NDC | 53208-502 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ZINC OXIDE, TITANIUM DIOXIDE, OCTINOXATE |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20100330 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | LG Household and Healthcare, Inc. |
| Substance Name | OCTINOXATE; TITANIUM DIOXIDE; ZINC OXIDE |
| Strength Number | 7.2; 4.03; 11.04 |
| Strength Unit | mL/100mL; mL/100mL; mL/100mL |
| Pharmaceutical Classes |
