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Cleanoz
Cleanoz - 44929-002-07 - (sodium chloride)
Drug Information of Cleanoz
| 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) |
Labeler Information of Cleanoz
| 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 Information of Cleanoz
| Package NDC: | 44929-002-07 |
| Package Description: | 30 AMPULE in 1 CARTON (44929-002-07) > 5 mL in 1 AMPULE (44929-002-01) |
NDC Information of Cleanoz
| NDC Code | 44929-002-07 |
| Proprietary Name | Cleanoz |
| Package Description | 30 AMPULE in 1 CARTON (44929-002-07) > 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 |
