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PRESCRIPTIVES
PRESCRIPTIVES - 59158-913-01 - (OCTINOXATE, TITANIUM DIOXIDE, and ZINC OXIDE)
Drug Information of PRESCRIPTIVES
| Product NDC: | 59158-913 |
| Proprietary Name: | PRESCRIPTIVES |
| Non Proprietary Name: | OCTINOXATE, TITANIUM DIOXIDE, and ZINC OXIDE |
| Active Ingredient(s): | .04551; .01554; .01665 g/mL; g/mL; g/mL & nbsp; OCTINOXATE, TITANIUM DIOXIDE, and ZINC OXIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of PRESCRIPTIVES
| Product NDC: | 59158-913 |
| Labeler Name: | PRESCRIPTIVES INC. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20061116 |
Package Information of PRESCRIPTIVES
| Package NDC: | 59158-913-01 |
| Package Description: | 1 TUBE in 1 CARTON (59158-913-01) > 3.5 mL in 1 TUBE |
NDC Information of PRESCRIPTIVES
| NDC Code | 59158-913-01 |
| Proprietary Name | PRESCRIPTIVES |
| Package Description | 1 TUBE in 1 CARTON (59158-913-01) > 3.5 mL in 1 TUBE |
| Product NDC | 59158-913 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE, TITANIUM DIOXIDE, and ZINC OXIDE |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20061116 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | PRESCRIPTIVES INC. |
| Substance Name | OCTINOXATE; TITANIUM DIOXIDE; ZINC OXIDE |
| Strength Number | .04551; .01554; .01665 |
| Strength Unit | g/mL; g/mL; g/mL |
| Pharmaceutical Classes |
