Product NDC: | 62032-108 |
Proprietary Name: | OBAGI-C RX SYSTEM C-EXFOLIATING DAY |
Non Proprietary Name: | OCTISALATE, OCTINOXATE, and OXYBENZONE |
Active Ingredient(s): | 75; 50; 40 mg/mL; mg/mL; mg/mL & nbsp; OCTISALATE, OCTINOXATE, and OXYBENZONE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 62032-108 |
Labeler Name: | OMP, INC. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20040101 |
Package NDC: | 62032-108-36 |
Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (62032-108-36) > 57 mL in 1 BOTTLE, PLASTIC |
NDC Code | 62032-108-36 |
Proprietary Name | OBAGI-C RX SYSTEM C-EXFOLIATING DAY |
Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (62032-108-36) > 57 mL in 1 BOTTLE, PLASTIC |
Product NDC | 62032-108 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | OCTISALATE, OCTINOXATE, and OXYBENZONE |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 20040101 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | OMP, INC. |
Substance Name | OCTINOXATE; OCTISALATE; OXYBENZONE |
Strength Number | 75; 50; 40 |
Strength Unit | mg/mL; mg/mL; mg/mL |
Pharmaceutical Classes |