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NA-ZONE
NA-ZONE - 58291-0011-1 - (SODIUM CHLORIDE)
Drug Information of NA-ZONE
| Product NDC: | 58291-0011 |
| Proprietary Name: | NA-ZONE |
| Non Proprietary Name: | SODIUM CHLORIDE |
| Active Ingredient(s): | .65 mL/100mL & nbsp; SODIUM CHLORIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of NA-ZONE
| Product NDC: | 58291-0011 |
| Labeler Name: | Snuva, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part349 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 19890101 |
Package Information of NA-ZONE
| Package NDC: | 58291-0011-1 |
| Package Description: | 59 mL in 1 BOTTLE (58291-0011-1) |
NDC Information of NA-ZONE
| NDC Code | 58291-0011-1 |
| Proprietary Name | NA-ZONE |
| Package Description | 59 mL in 1 BOTTLE (58291-0011-1) |
| Product NDC | 58291-0011 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | SODIUM CHLORIDE |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 19890101 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Snuva, Inc. |
| Substance Name | SODIUM CHLORIDE |
| Strength Number | .65 |
| Strength Unit | mL/100mL |
| Pharmaceutical Classes |
