| Product NDC: | 59915-4001 |
| Proprietary Name: | Conju Princess UV Sun Block |
| Non Proprietary Name: | ETHYLHEXYL METHOXYCINNAMATE |
| Active Ingredient(s): | .03; .05; .075; .0249; .01 mL/mL; mL/mL; mL/mL; mL/mL; mL/mL & nbsp; ETHYLHEXYL METHOXYCINNAMATE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 59915-4001 |
| Labeler Name: | Conju Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20101218 |
| Package NDC: | 59915-4001-1 |
| Package Description: | 1 mL in 1 POUCH (59915-4001-1) |
| NDC Code | 59915-4001-1 |
| Proprietary Name | Conju Princess UV Sun Block |
| Package Description | 1 mL in 1 POUCH (59915-4001-1) |
| Product NDC | 59915-4001 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ETHYLHEXYL METHOXYCINNAMATE |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20101218 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Conju Inc |
| Substance Name | AVOBENZONE; ENZACAMENE; OCTINOXATE; TITANIUM DIOXIDE; ZINC OXIDE |
| Strength Number | .03; .05; .075; .0249; .01 |
| Strength Unit | mL/mL; mL/mL; mL/mL; mL/mL; mL/mL |
| Pharmaceutical Classes |