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Absolute Finish Foundation SPF15
Absolute Finish Foundation SPF15 - 57913-2900-9 - (Octinoxate and Titanium Dioxide)
Drug Information of Absolute Finish Foundation SPF15
| Product NDC: | 57913-2900 |
| Proprietary Name: | Absolute Finish Foundation SPF15 |
| Non Proprietary Name: | Octinoxate and Titanium Dioxide |
| Active Ingredient(s): | 75; 20 mg/mL; mg/mL & nbsp; Octinoxate and Titanium Dioxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Absolute Finish Foundation SPF15
| Product NDC: | 57913-2900 |
| Labeler Name: | Erno Laszlo, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20130410 |
Package Information of Absolute Finish Foundation SPF15
| Package NDC: | 57913-2900-9 |
| Package Description: | 1 JAR in 1 CARTON (57913-2900-9) > 15 mL in 1 JAR |
NDC Information of Absolute Finish Foundation SPF15
| NDC Code | 57913-2900-9 |
| Proprietary Name | Absolute Finish Foundation SPF15 |
| Package Description | 1 JAR in 1 CARTON (57913-2900-9) > 15 mL in 1 JAR |
| Product NDC | 57913-2900 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Octinoxate and Titanium Dioxide |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20130410 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Erno Laszlo, Inc. |
| Substance Name | OCTINOXATE; TITANIUM DIOXIDE |
| Strength Number | 75; 20 |
| Strength Unit | mg/mL; mg/mL |
| Pharmaceutical Classes |
