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Aurum Metallicum
Aurum Metallicum - 53645-1020-0 - (Aurum Metallicum)
Drug Information of Aurum Metallicum
| Product NDC: | 53645-1020 |
| Proprietary Name: | Aurum Metallicum |
| Non Proprietary Name: | Aurum Metallicum |
| Active Ingredient(s): | 6 [hp_X]/50mL & nbsp; Aurum Metallicum |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Aurum Metallicum
| Product NDC: | 53645-1020 |
| Labeler Name: | True Botanica, LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 20130121 |
Package Information of Aurum Metallicum
| Package NDC: | 53645-1020-0 |
| Package Description: | 50 mL in 1 BOTTLE, WITH APPLICATOR (53645-1020-0) |
NDC Information of Aurum Metallicum
| NDC Code | 53645-1020-0 |
| Proprietary Name | Aurum Metallicum |
| Package Description | 50 mL in 1 BOTTLE, WITH APPLICATOR (53645-1020-0) |
| Product NDC | 53645-1020 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Aurum Metallicum |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20130121 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | True Botanica, LLC |
| Substance Name | GOLD |
| Strength Number | 6 |
| Strength Unit | [hp_X]/50mL |
| Pharmaceutical Classes |
