Product NDC: | 55878-105 |
Proprietary Name: | FACIAL CLEANSER |
Non Proprietary Name: | SALICYLIC ACID |
Active Ingredient(s): | .5 g/100mL & nbsp; SALICYLIC ACID |
Administration Route(s): | TOPICAL |
Dosage Form(s): | GEL |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 55878-105 |
Labeler Name: | Halogent, LLC (DBA Exposed Skin Care) |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333D |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20130207 |
Package NDC: | 55878-105-54 |
Package Description: | 1 BOTTLE in 1 BOX (55878-105-54) > 120 mL in 1 BOTTLE (55878-105-24) |
NDC Code | 55878-105-54 |
Proprietary Name | FACIAL CLEANSER |
Package Description | 1 BOTTLE in 1 BOX (55878-105-54) > 120 mL in 1 BOTTLE (55878-105-24) |
Product NDC | 55878-105 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | SALICYLIC ACID |
Dosage Form Name | GEL |
Route Name | TOPICAL |
Start Marketing Date | 20130207 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Halogent, LLC (DBA Exposed Skin Care) |
Substance Name | SALICYLIC ACID |
Strength Number | .5 |
Strength Unit | g/100mL |
Pharmaceutical Classes |