| 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 |