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Dermaroller Anhydrous Sunscreen
Dermaroller Anhydrous Sunscreen - 59958-201-01 - (Titanium Dioxide, Zinc Oxide)
Drug Information of Dermaroller Anhydrous Sunscreen
| Product NDC: | 59958-201 |
| Proprietary Name: | Dermaroller Anhydrous Sunscreen |
| 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 Dermaroller Anhydrous Sunscreen
| Product NDC: | 59958-201 |
| Labeler Name: | Owen Biosciences, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110301 |
Package Information of Dermaroller Anhydrous Sunscreen
| Package NDC: | 59958-201-01 |
| Package Description: | 30 g in 1 TUBE (59958-201-01) |
NDC Information of Dermaroller Anhydrous Sunscreen
| NDC Code | 59958-201-01 |
| Proprietary Name | Dermaroller Anhydrous Sunscreen |
| Package Description | 30 g in 1 TUBE (59958-201-01) |
| Product NDC | 59958-201 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Titanium Dioxide, Zinc Oxide |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20110301 |
| Marketing Category Name | OTC MONOGRAPH NOT 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 |
