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Sunkiss
Sunkiss - 41442-133-01 - (titanium dioxide and zinc oxide)
Drug Information of Sunkiss
| Product NDC: | 41442-133 |
| Proprietary Name: | Sunkiss |
| Non Proprietary Name: | titanium dioxide and zinc oxide |
| Active Ingredient(s): | .675; 3 mL/50mL; mL/50mL & nbsp; titanium dioxide and zinc oxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sunkiss
| Product NDC: | 41442-133 |
| Labeler Name: | Omorovicza Kozmetikai Kft |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110506 |
Package Information of Sunkiss
| Package NDC: | 41442-133-01 |
| Package Description: | 1 BOTTLE, GLASS in 1 BOX (41442-133-01) > 50 mL in 1 BOTTLE, GLASS |
NDC Information of Sunkiss
| NDC Code | 41442-133-01 |
| Proprietary Name | Sunkiss |
| Package Description | 1 BOTTLE, GLASS in 1 BOX (41442-133-01) > 50 mL in 1 BOTTLE, GLASS |
| Product NDC | 41442-133 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | titanium dioxide and zinc oxide |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20110506 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Omorovicza Kozmetikai Kft |
| Substance Name | TITANIUM DIOXIDE; ZINC OXIDE |
| Strength Number | .675; 3 |
| Strength Unit | mL/50mL; mL/50mL |
| Pharmaceutical Classes |
