Product NDC: | 24208-490 |
Proprietary Name: | Soothe XP |
Non Proprietary Name: | light mineral oil and mineral oil |
Active Ingredient(s): | .15; .675 mL/15mL; mL/15mL & nbsp; light mineral oil and mineral oil |
Administration Route(s): | OPHTHALMIC |
Dosage Form(s): | SOLUTION/ DROPS |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 24208-490 |
Labeler Name: | Baush & Lomb Incorporated |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part349 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20100826 |
Package NDC: | 24208-490-15 |
Package Description: | 1 BOTTLE, DROPPER in 1 BOX (24208-490-15) > 15 mL in 1 BOTTLE, DROPPER |
NDC Code | 24208-490-15 |
Proprietary Name | Soothe XP |
Package Description | 1 BOTTLE, DROPPER in 1 BOX (24208-490-15) > 15 mL in 1 BOTTLE, DROPPER |
Product NDC | 24208-490 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | light mineral oil and mineral oil |
Dosage Form Name | SOLUTION/ DROPS |
Route Name | OPHTHALMIC |
Start Marketing Date | 20100826 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Baush & Lomb Incorporated |
Substance Name | LIGHT MINERAL OIL; MINERAL OIL |
Strength Number | .15; .675 |
Strength Unit | mL/15mL; mL/15mL |
Pharmaceutical Classes |