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ULTRASOL
ULTRASOL - 59886-304-77 - (Titanium Dioxide, Zinc Oxide)
Drug Information of ULTRASOL
| Product NDC: | 59886-304 |
| Proprietary Name: | ULTRASOL |
| Non Proprietary Name: | Titanium Dioxide, Zinc Oxide |
| Active Ingredient(s): | 15; 8 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 ULTRASOL
| Product NDC: | 59886-304 |
| Labeler Name: | Fischer Pharmaceuticals Ltd |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20100610 |
Package Information of ULTRASOL
| Package NDC: | 59886-304-77 |
| Package Description: | 1 TUBE in 1 BOX (59886-304-77) > 50 g in 1 TUBE |
NDC Information of ULTRASOL
| NDC Code | 59886-304-77 |
| Proprietary Name | ULTRASOL |
| Package Description | 1 TUBE in 1 BOX (59886-304-77) > 50 g in 1 TUBE |
| Product NDC | 59886-304 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Titanium Dioxide, Zinc Oxide |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20100610 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Fischer Pharmaceuticals Ltd |
| Substance Name | TITANIUM DIOXIDE; ZINC OXIDE |
| Strength Number | 15; 8 |
| Strength Unit | g/100g; g/100g |
| Pharmaceutical Classes |
