| 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 |