Product NDC: | 24208-495 |
Proprietary Name: | Soothe |
Non Proprietary Name: | glycerin and propylene glycol |
Active Ingredient(s): | 6; 6 mg/mL; mg/mL & nbsp; glycerin and propylene glycol |
Administration Route(s): | OPHTHALMIC |
Dosage Form(s): | SOLUTION/ DROPS |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 24208-495 |
Labeler Name: | Bausch & Lomb Incorporated |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part349 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20100826 |
Package NDC: | 24208-495-28 |
Package Description: | 28 VIAL, SINGLE-USE in 1 CARTON (24208-495-28) > .6 mL in 1 VIAL, SINGLE-USE |
NDC Code | 24208-495-28 |
Proprietary Name | Soothe |
Package Description | 28 VIAL, SINGLE-USE in 1 CARTON (24208-495-28) > .6 mL in 1 VIAL, SINGLE-USE |
Product NDC | 24208-495 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | glycerin and propylene glycol |
Dosage Form Name | SOLUTION/ DROPS |
Route Name | OPHTHALMIC |
Start Marketing Date | 20100826 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Bausch & Lomb Incorporated |
Substance Name | GLYCERIN; PROPYLENE GLYCOL |
Strength Number | 6; 6 |
Strength Unit | mg/mL; mg/mL |
Pharmaceutical Classes |