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Complexion Brightener SPF20
Complexion Brightener SPF20 - 41442-123-01 - (Titanium dioxide and Zinc oxide)
Drug Information of Complexion Brightener SPF20
| Product NDC: | 41442-123 |
| Proprietary Name: | Complexion Brightener SPF20 |
| Non Proprietary Name: | Titanium dioxide and Zinc oxide |
| Active Ingredient(s): | .84; 2.1 mL/30mL; mL/30mL & nbsp; Titanium dioxide and Zinc oxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Complexion Brightener SPF20
| Product NDC: | 41442-123 |
| Labeler Name: | Omorovicza Kozmetikai Kft. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110301 |
Package Information of Complexion Brightener SPF20
| Package NDC: | 41442-123-01 |
| Package Description: | 1 BOTTLE, GLASS in 1 BOX (41442-123-01) > 30 mL in 1 BOTTLE, GLASS |
NDC Information of Complexion Brightener SPF20
| NDC Code | 41442-123-01 |
| Proprietary Name | Complexion Brightener SPF20 |
| Package Description | 1 BOTTLE, GLASS in 1 BOX (41442-123-01) > 30 mL in 1 BOTTLE, GLASS |
| Product NDC | 41442-123 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Titanium dioxide and Zinc oxide |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20110301 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Omorovicza Kozmetikai Kft. |
| Substance Name | TITANIUM DIOXIDE; ZINC OXIDE |
| Strength Number | .84; 2.1 |
| Strength Unit | mL/30mL; mL/30mL |
| Pharmaceutical Classes |
