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Dry Idea Advanced Dry-Powder Fresh
Dry Idea Advanced Dry-Powder Fresh - 54340-005-12 - (Aluminum Zirconium Pentachlorohydrex Gly)
Drug Information of Dry Idea Advanced Dry-Powder Fresh
| Product NDC: | 54340-005 |
| Proprietary Name: | Dry Idea Advanced Dry-Powder Fresh |
| Non Proprietary Name: | Aluminum Zirconium Pentachlorohydrex Gly |
| Active Ingredient(s): | 16.3 g/100mL & nbsp; Aluminum Zirconium Pentachlorohydrex Gly |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Dry Idea Advanced Dry-Powder Fresh
| Product NDC: | 54340-005 |
| Labeler Name: | The Dial Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part350 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20111018 |
Package Information of Dry Idea Advanced Dry-Powder Fresh
| Package NDC: | 54340-005-12 |
| Package Description: | 12 BOTTLE, PLASTIC in 1 BOX (54340-005-12) > 96.1 mL in 1 BOTTLE, PLASTIC (54340-005-32) |
NDC Information of Dry Idea Advanced Dry-Powder Fresh
| NDC Code | 54340-005-12 |
| Proprietary Name | Dry Idea Advanced Dry-Powder Fresh |
| Package Description | 12 BOTTLE, PLASTIC in 1 BOX (54340-005-12) > 96.1 mL in 1 BOTTLE, PLASTIC (54340-005-32) |
| Product NDC | 54340-005 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Aluminum Zirconium Pentachlorohydrex Gly |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20111018 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | The Dial Corporation |
| Substance Name | ALUMINUM ZIRCONIUM PENTACHLOROHYDREX GLY |
| Strength Number | 16.3 |
| Strength Unit | g/100mL |
| Pharmaceutical Classes |
