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GenTeal
GenTeal - 0078-0473-97 - (white petrolatum)
Drug Information of GenTeal
| Product NDC: | 0078-0473 |
| Proprietary Name: | GenTeal |
| Non Proprietary Name: | white petrolatum |
| Active Ingredient(s): | .15; .85 g/g; g/g & nbsp; white petrolatum |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of GenTeal
| Product NDC: | 0078-0473 |
| Labeler Name: | Novartis Pharmaceutical Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part349 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20091214 |
Package Information of GenTeal
| Package NDC: | 0078-0473-97 |
| Package Description: | 1 TUBE in 1 CARTON (0078-0473-97) > 3.5 g in 1 TUBE |
NDC Information of GenTeal
| NDC Code | 0078-0473-97 |
| Proprietary Name | GenTeal |
| Package Description | 1 TUBE in 1 CARTON (0078-0473-97) > 3.5 g in 1 TUBE |
| Product NDC | 0078-0473 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | white petrolatum |
| Dosage Form Name | OINTMENT |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 20091214 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Novartis Pharmaceutical Corporation |
| Substance Name | MINERAL OIL; PETROLATUM |
| Strength Number | .15; .85 |
| Strength Unit | g/g; g/g |
| Pharmaceutical Classes |
