Product NDC: | 54726-0100 |
Proprietary Name: | St. Ives Blemish and Blackhead control |
Non Proprietary Name: | Salicylic Acid |
Active Ingredient(s): | .02 g/g & nbsp; Salicylic Acid |
Administration Route(s): | TOPICAL |
Dosage Form(s): | EMULSION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 54726-0100 |
Labeler Name: | Cosmetic Laboratories of America |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333D |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20110223 |
Package NDC: | 54726-0100-1 |
Package Description: | 28 g in 1 TUBE (54726-0100-1) |
NDC Code | 54726-0100-1 |
Proprietary Name | St. Ives Blemish and Blackhead control |
Package Description | 28 g in 1 TUBE (54726-0100-1) |
Product NDC | 54726-0100 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Salicylic Acid |
Dosage Form Name | EMULSION |
Route Name | TOPICAL |
Start Marketing Date | 20110223 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Cosmetic Laboratories of America |
Substance Name | SALICYLIC ACID |
Strength Number | .02 |
Strength Unit | g/g |
Pharmaceutical Classes |