Product NDC: | 44929-002 |
Proprietary Name: | Cleanoz |
Non Proprietary Name: | sodium chloride |
Active Ingredient(s): | 900 mg/100mL & nbsp; sodium chloride |
Administration Route(s): | NASAL; OPHTHALMIC |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 44929-002 |
Labeler Name: | Laboratoires Gifrer Barbezat |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20081125 |
Package NDC: | 44929-002-03 |
Package Description: | 3 AMPULE in 1 CARTON (44929-002-03) > 5 mL in 1 AMPULE (44929-002-01) |
NDC Code | 44929-002-03 |
Proprietary Name | Cleanoz |
Package Description | 3 AMPULE in 1 CARTON (44929-002-03) > 5 mL in 1 AMPULE (44929-002-01) |
Product NDC | 44929-002 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | sodium chloride |
Dosage Form Name | SOLUTION |
Route Name | NASAL; OPHTHALMIC |
Start Marketing Date | 20081125 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Laboratoires Gifrer Barbezat |
Substance Name | SODIUM CHLORIDE |
Strength Number | 900 |
Strength Unit | mg/100mL |
Pharmaceutical Classes |