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EFFET PARFAIT
EFFET PARFAIT - 13537-023-08 - (Octinoxate and Titanium Dioxide)
Drug Information of EFFET PARFAIT
| Product NDC: | 13537-023 |
| Proprietary Name: | EFFET PARFAIT |
| Non Proprietary Name: | Octinoxate and Titanium Dioxide |
| Active Ingredient(s): | .065; .016 mL/mL; mL/mL & nbsp; Octinoxate and Titanium Dioxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of EFFET PARFAIT
| Product NDC: | 13537-023 |
| Labeler Name: | Ventura Corporation Ltd. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110810 |
Package Information of EFFET PARFAIT
| Package NDC: | 13537-023-08 |
| Package Description: | 1 BOTTLE in 1 CARTON (13537-023-08) > 40.5 mL in 1 BOTTLE (13537-023-07) |
NDC Information of EFFET PARFAIT
| NDC Code | 13537-023-08 |
| Proprietary Name | EFFET PARFAIT |
| Package Description | 1 BOTTLE in 1 CARTON (13537-023-08) > 40.5 mL in 1 BOTTLE (13537-023-07) |
| Product NDC | 13537-023 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Octinoxate and Titanium Dioxide |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20110810 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Ventura Corporation Ltd. |
| Substance Name | OCTINOXATE; TITANIUM DIOXIDE |
| Strength Number | .065; .016 |
| Strength Unit | mL/mL; mL/mL |
| Pharmaceutical Classes |
