| Product NDC: | 49743-3047 |
| Proprietary Name: | Mineral Oil, Petrolatum and Phenylephrine HCl |
| Non Proprietary Name: | mineral oil, petrolatum, phenylephrine HCl |
| Active Ingredient(s): | 140; 741; 2.5 mg/g; mg/g; mg/g & nbsp; mineral oil, petrolatum, phenylephrine HCl |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 49743-3047 |
| Labeler Name: | Axcentria Pharmaceuticals, LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part346 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20130628 |
| Package NDC: | 49743-3047-1 |
| Package Description: | 1 TUBE in 1 CARTON (49743-3047-1) > 56.8 g in 1 TUBE |
| NDC Code | 49743-3047-1 |
| Proprietary Name | Mineral Oil, Petrolatum and Phenylephrine HCl |
| Package Description | 1 TUBE in 1 CARTON (49743-3047-1) > 56.8 g in 1 TUBE |
| Product NDC | 49743-3047 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | mineral oil, petrolatum, phenylephrine HCl |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 20130628 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Axcentria Pharmaceuticals, LLC |
| Substance Name | MINERAL OIL; PETROLATUM; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 140; 741; 2.5 |
| Strength Unit | mg/g; mg/g; mg/g |
| Pharmaceutical Classes |