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Puralube
Puralube - 48102-017-35 - (Mineral oil and white petrolatum)
Drug Information of Puralube
| Product NDC: | 48102-017 |
| Proprietary Name: | Puralube |
| Non Proprietary Name: | Mineral oil and white petrolatum |
| Active Ingredient(s): | 150; 850 mg/g; mg/g & nbsp; Mineral oil and white petrolatum |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Puralube
| Product NDC: | 48102-017 |
| Labeler Name: | Fera Pharmaceuticals |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part349 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110202 |
Package Information of Puralube
| Package NDC: | 48102-017-35 |
| Package Description: | 1 TUBE in 1 CARTON (48102-017-35) > 3.5 g in 1 TUBE |
NDC Information of Puralube
| NDC Code | 48102-017-35 |
| Proprietary Name | Puralube |
| Package Description | 1 TUBE in 1 CARTON (48102-017-35) > 3.5 g in 1 TUBE |
| Product NDC | 48102-017 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Mineral oil and white petrolatum |
| Dosage Form Name | OINTMENT |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 20110202 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Fera Pharmaceuticals |
| Substance Name | MINERAL OIL; PETROLATUM |
| Strength Number | 150; 850 |
| Strength Unit | mg/g; mg/g |
| Pharmaceutical Classes |
