| Product NDC: | 66078-440 |
| Proprietary Name: | Sun Total Protector 30 broad spectrum SPF 30 daily protection |
| Non Proprietary Name: | Octinoxate, Octisalate, Zinc Oxide |
| Active Ingredient(s): | 7.5; 4; 7.8 g/100g; g/100g; g/100g & nbsp; Octinoxate, Octisalate, Zinc Oxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 66078-440 |
| Labeler Name: | MD Formulation. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20120815 |
| Package NDC: | 66078-440-03 |
| Package Description: | 10.8 g in 1 TUBE (66078-440-03) |
| NDC Code | 66078-440-03 |
| Proprietary Name | Sun Total Protector 30 broad spectrum SPF 30 daily protection |
| Package Description | 10.8 g in 1 TUBE (66078-440-03) |
| Product NDC | 66078-440 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Octinoxate, Octisalate, Zinc Oxide |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20120815 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | MD Formulation. |
| Substance Name | OCTINOXATE; OCTISALATE; ZINC OXIDE |
| Strength Number | 7.5; 4; 7.8 |
| Strength Unit | g/100g; g/100g; g/100g |
| Pharmaceutical Classes |