 
                        | 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 |