| Product NDC: | 43074-116 |
| Proprietary Name: | Acnecycline |
| Non Proprietary Name: | TETRACYCLINE HYDROCHLORIDE |
| Active Ingredient(s): | .03 mg/mL & nbsp; TETRACYCLINE HYDROCHLORIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 43074-116 |
| Labeler Name: | Phillips Company |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333B |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110215 |
| Package NDC: | 43074-116-02 |
| Package Description: | 1 BOTTLE, DROPPER in 1 BOTTLE, PLASTIC (43074-116-02) > 3 mL in 1 BOTTLE, DROPPER (43074-116-01) |
| NDC Code | 43074-116-02 |
| Proprietary Name | Acnecycline |
| Package Description | 1 BOTTLE, DROPPER in 1 BOTTLE, PLASTIC (43074-116-02) > 3 mL in 1 BOTTLE, DROPPER (43074-116-01) |
| Product NDC | 43074-116 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | TETRACYCLINE HYDROCHLORIDE |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 20110215 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Phillips Company |
| Substance Name | TETRACYCLINE HYDROCHLORIDE |
| Strength Number | .03 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |