FDA.reportPublic FDA data

PEMF Optimizer

Product NDC
43742-0693
11-digit product format
437420693
Labeler code
43742
Product ID
43742-0693_f7c780d6-6870-4f2a-b9bb-f01ac287ca90
Type
HUMAN OTC DRUG
Nonproprietary name
Aqua Sulis, Argentum Metallicum, Aurum Metallicum, 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
2015-12-08
Substance
CALCIUM HEXAFLUOROSILICATE; COPPER; GOLD; MANGANESE; SILVER; VANADIUM; VISCUM ALBUM FRUITING TOP; WATER; ZINC
Active strength
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
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
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
PEMF Optimizer
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
WATER1 [hp_M]/mL
SILVER1 [hp_M]/mL
GOLD1 [hp_M]/mL
COPPER1 [hp_M]/mL
CALCIUM HEXAFLUOROSILICATE1 [hp_M]/mL
MANGANESE1 [hp_M]/mL
VANADIUM1 [hp_M]/mL
VISCUM ALBUM FRUITING TOP30 [hp_C]/mL
ZINC1 [hp_M]/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 9 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
059QF0KO0RInternal UNII lookup
3M4G523W1GInternal UNII lookup
79Y1949PYOInternal UNII lookup
789U1901C5Internal UNII lookup
2NVP93XVQ3Internal UNII lookup
42Z2K6ZL8PInternal UNII lookup
00J9J9XKDEInternal UNII lookup
BK9092J5MPInternal UNII lookup
J41CSQ7QDSInternal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
97d57469-4c5b-4d3f-9398-3a1a6617a649Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c599c4a0-705d-4ebb-ab1f-977af038f96aProduct name120251124

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
43742-0693-1PEMF Optimizer30 mL in 1 BOTTLE, DROPPERLIQUID306

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
43742-0693PEMF OPTIMIZER (AQUA SULIS, ARGENTUM METALLICUM, AURUM METALLICUM, CUPRUM METALLICUM, LAPIS ALBUS, MANGANUM METALLICUM VANADIUM METALLICUM VISCUM ALBUM, ZINCUM METALLICUM) LIQUID [DESERET BIOLOGICALS, INC.]6Current NDC, Legacy NDC, 1 package rows20240425_97d57469-4c5b-4d3f-9398-3a1a6617a649.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
PEMF OptimizerAQUA SULIS, ARGENTUM METALLICUM, AURUM METALLICUM, CUPRUM METALLICUM, LAPIS ALBUS, MANGANUM METALLICUM VANADIUM METALLICUM VISCUM ALBUM, ZINCUM METALLICUMDeseret Biologicals, Inc.97d57469-4c5b-4d3f-9398-3a1a6617a6492024-04-23WarningsExact identifier
ndc (product): 43742-0693

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
43742-0693-14374206930130 mL in 1 BOTTLE, DROPPER (43742-0693-1) 30 ml2015-12-080000-00-00NoNoCurrent