Product NDC: | 43074-110 |
Proprietary Name: | Acneclir |
Non Proprietary Name: | SALICYLIC ACID |
Active Ingredient(s): | .02 mL/mL & nbsp; SALICYLIC ACID |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 43074-110 |
Labeler Name: | Phillips Company |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333D |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20101230 |
Package NDC: | 43074-110-29 |
Package Description: | 1 BOTTLE, DROPPER in 1 BOX (43074-110-29) > 3 mL in 1 BOTTLE, DROPPER (43074-110-27) |
NDC Code | 43074-110-29 |
Proprietary Name | Acneclir |
Package Description | 1 BOTTLE, DROPPER in 1 BOX (43074-110-29) > 3 mL in 1 BOTTLE, DROPPER (43074-110-27) |
Product NDC | 43074-110 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | SALICYLIC ACID |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 20101230 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Phillips Company |
Substance Name | SALICYLIC ACID |
Strength Number | .02 |
Strength Unit | mL/mL |
Pharmaceutical Classes |