| Product NDC: | 43742-0055 |
| Proprietary Name: | Polarity Plus |
| Non Proprietary Name: | Aqua solis, Argentum metallicum, Aurum metallicim, Cuprum metallicum, Lapis albus, Manganum metallicum, Vanadium metallicum, Viscum album, Zincum metallicum |
| Active Ingredient(s): | 1; 1; 1; 1; 1; 1; 1; 30; 1 [hp_M]/mL; [hp_M]/mL; [hp_M]/mL; [hp_M]/mL; [hp_M]/mL; [hp_M]/mL; [hp_M]/mL; [hp_C]/mL; [hp_M]/mL & nbsp; Aqua solis, Argentum metallicum, Aurum metallicim, Cuprum metallicum, Lapis albus, Manganum metallicum, Vanadium metallicum, Viscum album, Zincum metallicum |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 43742-0055 |
| Labeler Name: | Deseret Biologicals, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 20120607 |
| Package NDC: | 43742-0055-1 |
| Package Description: | 30 mL in 1 BOTTLE, DROPPER (43742-0055-1) |
| NDC Code | 43742-0055-1 |
| Proprietary Name | Polarity Plus |
| Package Description | 30 mL in 1 BOTTLE, DROPPER (43742-0055-1) |
| Product NDC | 43742-0055 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Aqua solis, Argentum metallicum, Aurum metallicim, Cuprum metallicum, Lapis albus, Manganum metallicum, Vanadium metallicum, Viscum album, Zincum metallicum |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20120607 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | Deseret Biologicals, Inc. |
| Substance Name | CALCIUM HEXAFLUOROSILICATE; COPPER; GOLD; MANGANESE; SILVER; VANADIUM; VISCUM ALBUM FRUITING TOP; WATER; ZINC |
| Strength Number | 1; 1; 1; 1; 1; 1; 1; 30; 1 |
| Strength Unit | [hp_M]/mL; [hp_M]/mL; [hp_M]/mL; [hp_M]/mL; [hp_M]/mL; [hp_M]/mL; [hp_M]/mL; [hp_C]/mL; [hp_M]/mL |
| Pharmaceutical Classes |