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Natria
Natria - 44717-535-02 - (Salicylic Acid)
Drug Information of Natria
| Product NDC: | 44717-535 |
| Proprietary Name: | Natria |
| Non Proprietary Name: | Salicylic Acid |
| Active Ingredient(s): | 30 mL/100mL & nbsp; Salicylic Acid |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Natria
| Product NDC: | 44717-535 |
| Labeler Name: | Wasatch Product Development, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20100628 |
Package Information of Natria
| Package NDC: | 44717-535-02 |
| Package Description: | 1 TUBE in 1 BOX (44717-535-02) > 30 mL in 1 TUBE (44717-535-01) |
NDC Information of Natria
| NDC Code | 44717-535-02 |
| Proprietary Name | Natria |
| Package Description | 1 TUBE in 1 BOX (44717-535-02) > 30 mL in 1 TUBE (44717-535-01) |
| Product NDC | 44717-535 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Salicylic Acid |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20100628 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Wasatch Product Development, Inc. |
| Substance Name | SALICYLIC ACID |
| Strength Number | 30 |
| Strength Unit | mL/100mL |
| Pharmaceutical Classes |
