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Anhydrous SPF 30
Anhydrous SPF 30 - 59958-200-01 - (Titanium Dioxide, Zinc Oxide)
Drug Information of Anhydrous SPF 30
| 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) |
Labeler Information of Anhydrous SPF 30
| 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 Information of Anhydrous SPF 30
| Package NDC: | 59958-200-01 |
| Package Description: | 100000 g in 1 DRUM (59958-200-01) |
NDC Information of Anhydrous SPF 30
| NDC Code | 59958-200-01 |
| Proprietary Name | Anhydrous SPF 30 |
| Package Description | 100000 g in 1 DRUM (59958-200-01) |
| 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 |
