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 |