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Aluminum Acetate Astringent
Aluminum Acetate Astringent - 51224-153-24 - (Calcium Acetate and Aluminum sulfate)
Drug Information of Aluminum Acetate Astringent
| Product NDC: | 51224-153 |
| Proprietary Name: | Aluminum Acetate Astringent |
| Non Proprietary Name: | Calcium Acetate and Aluminum sulfate |
| Active Ingredient(s): | 1191; 839 mg/2030mg; mg/2030mg & nbsp; Calcium Acetate and Aluminum sulfate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | POWDER, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Aluminum Acetate Astringent
| Product NDC: | 51224-153 |
| Labeler Name: | TAGI Pharma Incorporated |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part347 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110615 |
Package Information of Aluminum Acetate Astringent
| Package NDC: | 51224-153-24 |
| Package Description: | 12 BOX in 1 CARTON (51224-153-24) > 12 POUCH in 1 BOX (51224-153-12) > 2030 mg in 1 POUCH (51224-153-99) |
NDC Information of Aluminum Acetate Astringent
| NDC Code | 51224-153-24 |
| Proprietary Name | Aluminum Acetate Astringent |
| Package Description | 12 BOX in 1 CARTON (51224-153-24) > 12 POUCH in 1 BOX (51224-153-12) > 2030 mg in 1 POUCH (51224-153-99) |
| Product NDC | 51224-153 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Calcium Acetate and Aluminum sulfate |
| Dosage Form Name | POWDER, FOR SOLUTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20110615 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | TAGI Pharma Incorporated |
| Substance Name | ALUMINUM SULFATE; CALCIUM ACETATE |
| Strength Number | 1191; 839 |
| Strength Unit | mg/2030mg; mg/2030mg |
| Pharmaceutical Classes |
