Product NDC: | 76358-194 |
Proprietary Name: | Santalia Clinical Daily Serum |
Non Proprietary Name: | Salicylic Acid |
Active Ingredient(s): | .54 g/100mL & nbsp; Salicylic Acid |
Administration Route(s): | TOPICAL |
Dosage Form(s): | GEL |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 76358-194 |
Labeler Name: | Santalis Pharmaceuticals |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333D |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20130101 |
Package NDC: | 76358-194-02 |
Package Description: | 1 TUBE in 1 CARTON (76358-194-02) > 30 mL in 1 TUBE (76358-194-01) |
NDC Code | 76358-194-02 |
Proprietary Name | Santalia Clinical Daily Serum |
Package Description | 1 TUBE in 1 CARTON (76358-194-02) > 30 mL in 1 TUBE (76358-194-01) |
Product NDC | 76358-194 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Salicylic Acid |
Dosage Form Name | GEL |
Route Name | TOPICAL |
Start Marketing Date | 20130101 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Santalis Pharmaceuticals |
Substance Name | SALICYLIC ACID |
Strength Number | .54 |
Strength Unit | g/100mL |
Pharmaceutical Classes |