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Tucks Hemorrhoidal
Tucks Hemorrhoidal - 30014-100-01 - (Mineral Oil, Pramoxine Hydrochloride, and Zinc Oxide)
Drug Information of Tucks Hemorrhoidal
| Product NDC: | 30014-100 |
| Proprietary Name: | Tucks Hemorrhoidal |
| Non Proprietary Name: | Mineral Oil, Pramoxine Hydrochloride, and Zinc Oxide |
| Active Ingredient(s): | 466; 10; 125 mg/g; mg/g; mg/g & nbsp; Mineral Oil, Pramoxine Hydrochloride, and Zinc Oxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Tucks Hemorrhoidal
| Product NDC: | 30014-100 |
| Labeler Name: | McNEIL-PPC, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part346 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20120730 |
Package Information of Tucks Hemorrhoidal
| Package NDC: | 30014-100-01 |
| Package Description: | 1 TUBE in 1 CARTON (30014-100-01) > 28.3 g in 1 TUBE |
NDC Information of Tucks Hemorrhoidal
| NDC Code | 30014-100-01 |
| Proprietary Name | Tucks Hemorrhoidal |
| Package Description | 1 TUBE in 1 CARTON (30014-100-01) > 28.3 g in 1 TUBE |
| Product NDC | 30014-100 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Mineral Oil, Pramoxine Hydrochloride, and Zinc Oxide |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 20120730 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | McNEIL-PPC, Inc. |
| Substance Name | MINERAL OIL; PRAMOXINE HYDROCHLORIDE; ZINC OXIDE |
| Strength Number | 466; 10; 125 |
| Strength Unit | mg/g; mg/g; mg/g |
| Pharmaceutical Classes |
