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Dermadrox
Dermadrox - 54162-221-01 - (Aluminum Hydroxide)
Drug Information of Dermadrox
| Product NDC: | 54162-221 |
| Proprietary Name: | Dermadrox |
| Non Proprietary Name: | Aluminum Hydroxide |
| Active Ingredient(s): | 1.2 g/100g & nbsp; Aluminum Hydroxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Dermadrox
| Product NDC: | 54162-221 |
| Labeler Name: | GERITREX CORP |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part346 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20130130 |
Package Information of Dermadrox
| Package NDC: | 54162-221-01 |
| Package Description: | 113 g in 1 TUBE (54162-221-01) |
NDC Information of Dermadrox
| NDC Code | 54162-221-01 |
| Proprietary Name | Dermadrox |
| Package Description | 113 g in 1 TUBE (54162-221-01) |
| Product NDC | 54162-221 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Aluminum Hydroxide |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 20130130 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | GERITREX CORP |
| Substance Name | ALUMINUM HYDROXIDE |
| Strength Number | 1.2 |
| Strength Unit | g/100g |
| Pharmaceutical Classes |
