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LBEL EFFET PARFAIT
LBEL EFFET PARFAIT - 13537-434-02 - (Octinoxate and Titanium Dioxide)
Drug Information of LBEL EFFET PARFAIT
| Product NDC: | 13537-434 |
| Proprietary Name: | LBEL EFFET PARFAIT |
| Non Proprietary Name: | Octinoxate and Titanium Dioxide |
| Active Ingredient(s): | .07; .024 g/mL; g/mL & nbsp; Octinoxate and Titanium Dioxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of LBEL EFFET PARFAIT
| Product NDC: | 13537-434 |
| Labeler Name: | Ventura Corporation LTD. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20120914 |
Package Information of LBEL EFFET PARFAIT
| Package NDC: | 13537-434-02 |
| Package Description: | 1 BOTTLE in 1 BOX (13537-434-02) > 1 mL in 1 BOTTLE (13537-434-01) |
NDC Information of LBEL EFFET PARFAIT
| NDC Code | 13537-434-02 |
| Proprietary Name | LBEL EFFET PARFAIT |
| Package Description | 1 BOTTLE in 1 BOX (13537-434-02) > 1 mL in 1 BOTTLE (13537-434-01) |
| Product NDC | 13537-434 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Octinoxate and Titanium Dioxide |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20120914 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Ventura Corporation LTD. |
| Substance Name | OCTINOXATE; TITANIUM DIOXIDE |
| Strength Number | .07; .024 |
| Strength Unit | g/mL; g/mL |
| Pharmaceutical Classes |
