Polarity Plus
- Product NDC
- 43742-0055
- 11-digit product format
- 437420055
- Labeler code
- 43742
- Product ID
- 43742-0055_c2e81ff8-b2f8-4b69-bd16-5b8b2d18c2d8
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Aqua solis, Argentum metallicum, Aurum metallicim, Cuprum metallicum, Lapis albus, Manganum metallicum, Vanadium metallicum, Viscum album, Zincum metallicum
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Deseret Biologicals, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2012-06-07
- Marketing end
- 2022-11-30
- Substance
- CALCIUM HEXAFLUOROSILICATE; COPPER; GOLD; MANGANESE; SILVER; VANADIUM; VISCUM ALBUM FRUITING TOP; WATER; ZINC
- Active strength
- 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
- Pharmacologic classes
- Allergens [CS], Cell-mediated Immunity [PE], Copper [CS], Copper-containing Intrauterine Device [EPC], Decreased Embryonic Implantation [PE], Decreased Sperm Motility [PE], Increased Histamine Release [PE], Inhibit Ovum Fertilization [PE], Standardized Chemical Allergen [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 43742-0055-1 | 43742005501 | 30 mL in 1 BOTTLE, DROPPER (43742-0055-1) | 30 ml | 2012-06-07 | 2022-11-30 | No | No | Current |