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Suave
Suave - 64942-1139-1 - (Aluminum Zirconium Tetrachlorohydrex GLY)
Drug Information of Suave
| Product NDC: | 64942-1139 |
| Proprietary Name: | Suave |
| Non Proprietary Name: | Aluminum Zirconium Tetrachlorohydrex GLY |
| Active Ingredient(s): | 22 mL/100mL & nbsp; Aluminum Zirconium Tetrachlorohydrex GLY |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Suave
| Product NDC: | 64942-1139 |
| Labeler Name: | Conopco Inc. d/b/a Unilever |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part350 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20101118 |
Package Information of Suave
| Package NDC: | 64942-1139-1 |
| Package Description: | 80 mL in 1 CONTAINER (64942-1139-1) |
NDC Information of Suave
| NDC Code | 64942-1139-1 |
| Proprietary Name | Suave |
| Package Description | 80 mL in 1 CONTAINER (64942-1139-1) |
| Product NDC | 64942-1139 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Aluminum Zirconium Tetrachlorohydrex GLY |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20101118 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Conopco Inc. d/b/a Unilever |
| Substance Name | ALUMINUM CHLOROHYDRATE |
| Strength Number | 22 |
| Strength Unit | mL/100mL |
| Pharmaceutical Classes |
