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Sunmark Hemorrhoidal
Sunmark Hemorrhoidal - 49348-799-32 - (glycerin, phenylephrine HCl, pramoxine HCl, white petrolatum)
Drug Information of Sunmark Hemorrhoidal
| Product NDC: | 49348-799 |
| Proprietary Name: | Sunmark Hemorrhoidal |
| Non Proprietary Name: | glycerin, phenylephrine HCl, pramoxine HCl, white petrolatum |
| Active Ingredient(s): | 14.4; 15; .25; 1 g/100g; g/100g; g/100g; g/100g & nbsp; glycerin, phenylephrine HCl, pramoxine HCl, white petrolatum |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sunmark Hemorrhoidal
| Product NDC: | 49348-799 |
| Labeler Name: | McKesson |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part346 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20080204 |
Package Information of Sunmark Hemorrhoidal
| Package NDC: | 49348-799-32 |
| Package Description: | 1 TUBE in 1 CARTON (49348-799-32) > 51 g in 1 TUBE |
NDC Information of Sunmark Hemorrhoidal
| NDC Code | 49348-799-32 |
| Proprietary Name | Sunmark Hemorrhoidal |
| Package Description | 1 TUBE in 1 CARTON (49348-799-32) > 51 g in 1 TUBE |
| Product NDC | 49348-799 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | glycerin, phenylephrine HCl, pramoxine HCl, white petrolatum |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20080204 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | McKesson |
| Substance Name | GLYCERIN; PETROLATUM; PHENYLEPHRINE HYDROCHLORIDE; PRAMOXINE HYDROCHLORIDE |
| Strength Number | 14.4; 15; .25; 1 |
| Strength Unit | g/100g; g/100g; g/100g; g/100g |
| Pharmaceutical Classes |
