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Luminous Intensive Decollote Treatment SPF 20
Luminous Intensive Decollote Treatment SPF 20 - 57913-2815-0 - (Avobenzone, Octinoxate, and Octisalate)
Drug Information of Luminous Intensive Decollote Treatment SPF 20
| Product NDC: | 57913-2815 |
| Proprietary Name: | Luminous Intensive Decollote Treatment SPF 20 |
| Non Proprietary Name: | Avobenzone, Octinoxate, and Octisalate |
| Active Ingredient(s): | 20; 75; 50 mg/mL; mg/mL; mg/mL & nbsp; Avobenzone, Octinoxate, and Octisalate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Luminous Intensive Decollote Treatment SPF 20
| Product NDC: | 57913-2815 |
| 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 Luminous Intensive Decollote Treatment SPF 20
| Package NDC: | 57913-2815-0 |
| Package Description: | 1 JAR in 1 CARTON (57913-2815-0) > 50 mL in 1 JAR |
NDC Information of Luminous Intensive Decollote Treatment SPF 20
| NDC Code | 57913-2815-0 |
| Proprietary Name | Luminous Intensive Decollote Treatment SPF 20 |
| Package Description | 1 JAR in 1 CARTON (57913-2815-0) > 50 mL in 1 JAR |
| Product NDC | 57913-2815 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Avobenzone, Octinoxate, and Octisalate |
| 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 | AVOBENZONE; OCTINOXATE; OCTISALATE |
| Strength Number | 20; 75; 50 |
| Strength Unit | mg/mL; mg/mL; mg/mL |
| Pharmaceutical Classes |
