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REFRESH LACRI-LUBE
REFRESH LACRI-LUBE - 0023-0312-07 - (mineral oil, petrolatum)
Drug Information of REFRESH LACRI-LUBE
| Product NDC: | 0023-0312 |
| Proprietary Name: | REFRESH LACRI-LUBE |
| Non Proprietary Name: | mineral oil, petrolatum |
| Active Ingredient(s): | 425; 568 mg/g; mg/g & nbsp; mineral oil, petrolatum |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of REFRESH LACRI-LUBE
| Product NDC: | 0023-0312 |
| Labeler Name: | Allergan, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part349 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 19771215 |
Package Information of REFRESH LACRI-LUBE
| Package NDC: | 0023-0312-07 |
| Package Description: | 1 TUBE in 1 CARTON (0023-0312-07) > 7 g in 1 TUBE |
NDC Information of REFRESH LACRI-LUBE
| NDC Code | 0023-0312-07 |
| Proprietary Name | REFRESH LACRI-LUBE |
| Package Description | 1 TUBE in 1 CARTON (0023-0312-07) > 7 g in 1 TUBE |
| Product NDC | 0023-0312 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | mineral oil, petrolatum |
| Dosage Form Name | OINTMENT |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 19771215 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Allergan, Inc. |
| Substance Name | MINERAL OIL; PETROLATUM |
| Strength Number | 425; 568 |
| Strength Unit | mg/g; mg/g |
| Pharmaceutical Classes |
