Product NDC: | 51325-200 |
Proprietary Name: | Rejuvaderm Medispa Body |
Non Proprietary Name: | Octinoxate, octisalate, oxybenzone |
Active Ingredient(s): | 26.625; 17.75; 10.65 mL/355mL; mL/355mL; mL/355mL & nbsp; Octinoxate, octisalate, oxybenzone |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 51325-200 |
Labeler Name: | Ellen H Frankle MD Inc |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20100801 |
Package NDC: | 51325-200-02 |
Package Description: | 355 mL in 1 BOTTLE (51325-200-02) |
NDC Code | 51325-200-02 |
Proprietary Name | Rejuvaderm Medispa Body |
Package Description | 355 mL in 1 BOTTLE (51325-200-02) |
Product NDC | 51325-200 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Octinoxate, octisalate, oxybenzone |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 20100801 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Ellen H Frankle MD Inc |
Substance Name | OCTINOXATE; OCTISALATE; OXYBENZONE |
Strength Number | 26.625; 17.75; 10.65 |
Strength Unit | mL/355mL; mL/355mL; mL/355mL |
Pharmaceutical Classes |