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: | 21695-681-07 |
Package Description: | 7 g in 1 TUBE (21695-681-07) |
NDC Code | 21695-681-07 |
Proprietary Name | Mineral Oil |
Package Description | 7 g in 1 TUBE (21695-681-07) |
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 |