Product NDC: | 42248-129 |
Proprietary Name: | Whitening |
Non Proprietary Name: | OCTINOXATE avobenzone titanium oxide |
Active Ingredient(s): | 1.5; 3.5; 12.5 mL/50mL; mL/50mL; mL/50mL & nbsp; OCTINOXATE avobenzone titanium oxide |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 42248-129 |
Labeler Name: | Zenith Medicosm SL |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20110815 |
Package NDC: | 42248-129-02 |
Package Description: | 1 JAR in 1 BOX (42248-129-02) > 50 mL in 1 JAR |
NDC Code | 42248-129-02 |
Proprietary Name | Whitening |
Package Description | 1 JAR in 1 BOX (42248-129-02) > 50 mL in 1 JAR |
Product NDC | 42248-129 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | OCTINOXATE avobenzone titanium oxide |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20110815 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Zenith Medicosm SL |
Substance Name | AVOBENZONE; OCTINOXATE; TITANIUM DIOXIDE |
Strength Number | 1.5; 3.5; 12.5 |
Strength Unit | mL/50mL; mL/50mL; mL/50mL |
Pharmaceutical Classes |