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 |