Home FDA labels 762c7ffb-6fc5-420f-972c-473a8169d92d Electrolyte Plus openFDA label record# This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)
Brand name Electrolyte Plus
Generic name BORON CITRATE, CALCIUM GLUCONATE, CHROMIUM PICOLINATE, COBALT GLUCONATE, COPPER GLUCONATE, FERROUS MURIATICUM, MAGNESIUM GLUCONICUM DIHYDRICUM, MANGANESE GLUCONATE, POTASSIUM GLUCONATE, SELENIUM DIOXIDE, SODIUM GLUCONATE, ZINCUM GLUCONICUM, KALI PHOSPHORICUM, NICCOLUM METALLICUM, VANADIUM METALLICUM, CALCAREA PHOSPHORICA
Manufacturer Deseret Biologicals, Inc.
Product type HUMAN OTC DRUG
SPL set ID abeb996b-c754-4455-b4d4-eba514fdbcad
SPL ID 762c7ffb-6fc5-420f-972c-473a8169d92d
Version 4
Effective date 2023-10-11
Source export date 2026-10-12
Source partition 10
Source file https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-10-12/befa34274042a52f589b22fe2add0b1c6f0a385c96447c28303de164bb144af5/drug-label-0010-of-0014.json.zip
Source manifest SHA-256 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run 20261013T011858Z
Imported at 2026-10-13 02:29:11 Harmonized routes table Harmonized routes ORAL
Harmonized identifier links# Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
Harmonized identifiers page 1 of 1 · 24 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Electrolyte Plus openfda.brand_name generic name BORON CITRATE, CALCIUM GLUCONATE, CHROMIUM PICOLINATE, COBALT GLUCONATE, COPPER GLUCONATE, FERROUS MURIATICUM, MAGNESIUM GLUCONICUM DIHYDRICUM, MANGANESE GLUCONATE, POTASSIUM GLUCONATE, SELENIUM DIOXIDE, SODIUM GLUCONATE, ZINCUM GLUCONICUM, KALI PHOSPHORICUM, NICCOLUM METALLICUM, VANADIUM METALLICUM, CALCAREA PHOSPHORICA openfda.generic_name manufacturer name Deseret Biologicals, Inc. openfda.manufacturer_name ndc package 43742-1516-1 openfda.package_ndc ndc product 43742-1516 openfda.product_ndc ndc11 package 43742151601 derived:openfda.package_ndc spl id 762c7ffb-6fc5-420f-972c-473a8169d92d id spl set id abeb996b-c754-4455-b4d4-eba514fdbcad set_id unii S71T8B8Z6P openfda.unii unii 9YY2F980SV openfda.unii unii CI71S98N1Z openfda.unii unii T42NAD2KHC openfda.unii unii 12H3K5QKN9 openfda.unii unii R6Q3791S76 openfda.unii unii SQE6VB453K openfda.unii unii S043P4DV22 openfda.unii unii RV823G6G67 openfda.unii unii 91D9GV0Z28 openfda.unii unii 26SK597UWV openfda.unii unii 0I2XIN602U openfda.unii unii 7OV03QG267 openfda.unii unii 00J9J9XKDE openfda.unii unii U6WSN5SQ1Z openfda.unii unii 9N3UK29E57 openfda.unii
Warnings cross-check# openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Warnings sections page 1 of 1 · 1 matching rows.
warnings WARNINGS: Keep out of reach of children. In case of overdose, contact physician or Poison Control Center right away. If pregnant or breast-feeding, seek advice of a health professional before use. Tamper seal: "Sealed for Your Protection." Do not use if seal is broken or missing.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.