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Dermectin Sunscreen
Dermectin Sunscreen - 59088-942-08 - (Titanium Dioxide)
Drug Information of Dermectin Sunscreen
| Product NDC: | 59088-942 |
| Proprietary Name: | Dermectin Sunscreen |
| Non Proprietary Name: | Titanium Dioxide |
| Active Ingredient(s): | 71 uL/mL & nbsp; Titanium Dioxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Dermectin Sunscreen
| Product NDC: | 59088-942 |
| Labeler Name: | PureTek Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110712 |
Package Information of Dermectin Sunscreen
| Package NDC: | 59088-942-08 |
| Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (59088-942-08) > 118 mL in 1 BOTTLE, PLASTIC |
NDC Information of Dermectin Sunscreen
| NDC Code | 59088-942-08 |
| Proprietary Name | Dermectin Sunscreen |
| Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (59088-942-08) > 118 mL in 1 BOTTLE, PLASTIC |
| Product NDC | 59088-942 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Titanium Dioxide |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20110712 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | PureTek Corporation |
| Substance Name | TITANIUM DIOXIDE |
| Strength Number | 71 |
| Strength Unit | uL/mL |
| Pharmaceutical Classes |
