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 |