| Product NDC: | 21695-681 |
| Proprietary Name: | Mineral Oil |
| Non Proprietary Name: | Lacri-Lube |
| Active Ingredient(s): | 425; 568 mg/g; mg/g & nbsp; Lacri-Lube |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 21695-681 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part346 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20071130 |
| Package NDC: | 21695-681-35 |
| Package Description: | 3.5 g in 1 TUBE (21695-681-35) |
| NDC Code | 21695-681-35 |
| Proprietary Name | Mineral Oil |
| Package Description | 3.5 g in 1 TUBE (21695-681-35) |
| Product NDC | 21695-681 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Lacri-Lube |
| Dosage Form Name | OINTMENT |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 20071130 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | MINERAL OIL; PETROLATUM |
| Strength Number | 425; 568 |
| Strength Unit | mg/g; mg/g |
| Pharmaceutical Classes |