Product NDC: | 66078-505 |
Proprietary Name: | Sun Total Protector Color 30 Dark Tint |
Non Proprietary Name: | Sun Total Protector Color 30 Dark Tint |
Active Ingredient(s): | 7.5; 4; 7.8 mL/100mL; mL/100mL; mL/100mL & nbsp; Sun Total Protector Color 30 Dark Tint |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 66078-505 |
Labeler Name: | MD Formulations |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20070520 |
Package NDC: | 66078-505-25 |
Package Description: | 42 CARTON in 1 CASE (66078-505-25) > 1 BOTTLE in 1 CARTON > 75 mL in 1 BOTTLE |
NDC Code | 66078-505-25 |
Proprietary Name | Sun Total Protector Color 30 Dark Tint |
Package Description | 42 CARTON in 1 CASE (66078-505-25) > 1 BOTTLE in 1 CARTON > 75 mL in 1 BOTTLE |
Product NDC | 66078-505 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Sun Total Protector Color 30 Dark Tint |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20070520 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | MD Formulations |
Substance Name | OCTINOXATE; OCTISALATE; ZINC OXIDE |
Strength Number | 7.5; 4; 7.8 |
Strength Unit | mL/100mL; mL/100mL; mL/100mL |
Pharmaceutical Classes |