Product NDC: | 49527-825 |
Proprietary Name: | ACNE SOLUTIONS |
Non Proprietary Name: | SALICYLIC ACID |
Active Ingredient(s): | .5 mL/100mL & nbsp; SALICYLIC ACID |
Administration Route(s): | TOPICAL |
Dosage Form(s): | GEL |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 49527-825 |
Labeler Name: | CLINIQUE LABORATORIES INC |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333D |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20081201 |
Package NDC: | 49527-825-01 |
Package Description: | 1 TUBE in 1 CARTON (49527-825-01) > 15 mL in 1 TUBE (49527-825-02) |
NDC Code | 49527-825-01 |
Proprietary Name | ACNE SOLUTIONS |
Package Description | 1 TUBE in 1 CARTON (49527-825-01) > 15 mL in 1 TUBE (49527-825-02) |
Product NDC | 49527-825 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | SALICYLIC ACID |
Dosage Form Name | GEL |
Route Name | TOPICAL |
Start Marketing Date | 20081201 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | CLINIQUE LABORATORIES INC |
Substance Name | SALICYLIC ACID |
Strength Number | .5 |
Strength Unit | mL/100mL |
Pharmaceutical Classes |