| Product NDC: | 66078-503 |
| Proprietary Name: | Sun Total Protector Color 30 Light Tint |
| Non Proprietary Name: | Zinc Oxide, Octisalate, Octinoxate |
| Active Ingredient(s): | 7.5; 4; 7.8 mL/100mL; mL/100mL; mL/100mL & nbsp; Zinc Oxide, Octisalate, Octinoxate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 66078-503 |
| 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: | 66078-503-25 |
| Package Description: | 42 CARTON in 1 CASE (66078-503-25) > 1 BOTTLE in 1 CARTON > 75 mL in 1 BOTTLE |
| NDC Code | 66078-503-25 |
| Proprietary Name | Sun Total Protector Color 30 Light Tint |
| Package Description | 42 CARTON in 1 CASE (66078-503-25) > 1 BOTTLE in 1 CARTON > 75 mL in 1 BOTTLE |
| Product NDC | 66078-503 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Zinc Oxide, Octisalate, Octinoxate |
| 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 |