Product NDC: | 59958-200 |
Proprietary Name: | Anhydrous SPF 30 |
Non Proprietary Name: | Titanium Dioxide, Zinc Oxide |
Active Ingredient(s): | 10.2; 3.7 g/100g; g/100g & nbsp; Titanium Dioxide, Zinc Oxide |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 59958-200 |
Labeler Name: | Owen Biosciences, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20090901 |
Package NDC: | 59958-200-02 |
Package Description: | 30 g in 1 TUBE (59958-200-02) |
NDC Code | 59958-200-02 |
Proprietary Name | Anhydrous SPF 30 |
Package Description | 30 g in 1 TUBE (59958-200-02) |
Product NDC | 59958-200 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Titanium Dioxide, Zinc Oxide |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20090901 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Owen Biosciences, Inc. |
Substance Name | TITANIUM DIOXIDE; ZINC OXIDE |
Strength Number | 10.2; 3.7 |
Strength Unit | g/100g; g/100g |
Pharmaceutical Classes |