Home FDA labels 0e768a0e-1c63-7a5b-e063-6394a90a8097 B13 CELL SALT COMPLEX 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 B13 CELL SALT COMPLEX
Generic name ALLIUM SATIVUM, AVENA SATIVA, CALCAREA CARBONICA, CALCAREA FLUORICA, CALCAREA PHOSPHORICA, CALCAREA SULPHURICA, CARBO VEGETABILIS, FERRUM IODATUM, HYPERICUM PERFORATUM, KALI PHOSPHORICUM, LACTICUM ACIDUM, MAGNESIA PHOSPHORICA, NATRUM MURIATICUM, NATRUM PHOSPHORICUM, PHOSPHORICUM ACIDUM, URTICA URENS
Manufacturer Apex Energetics Inc.
Product type HUMAN OTC DRUG
SPL set ID bf78b0b0-5b7b-28cb-e053-2a95a90a1e7d
SPL ID 0e768a0e-1c63-7a5b-e063-6394a90a8097
Version 2
Effective date 2024-01-08
Source export date 2026-09-28
Source partition 8
Source file https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 05:55:57 Harmonized routes table Harmonized routes SUBLINGUAL
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 B13 CELL SALT COMPLEX openfda.brand_name generic name ALLIUM SATIVUM, AVENA SATIVA, CALCAREA CARBONICA, CALCAREA FLUORICA, CALCAREA PHOSPHORICA, CALCAREA SULPHURICA, CARBO VEGETABILIS, FERRUM IODATUM, HYPERICUM PERFORATUM, KALI PHOSPHORICUM, LACTICUM ACIDUM, MAGNESIA PHOSPHORICA, NATRUM MURIATICUM, NATRUM PHOSPHORICUM, PHOSPHORICUM ACIDUM, URTICA URENS openfda.generic_name manufacturer name Apex Energetics Inc. openfda.manufacturer_name ndc package 63479-0213-1 openfda.package_ndc ndc product 63479-0213 openfda.product_ndc ndc11 package 63479021301 derived:openfda.package_ndc spl id 0e768a0e-1c63-7a5b-e063-6394a90a8097 id spl set id bf78b0b0-5b7b-28cb-e053-2a95a90a1e7d set_id unii 2P3VWU3H10 openfda.unii unii E934B3V59H openfda.unii unii V1V998DC17 openfda.unii unii CI71S98N1Z openfda.unii unii XK4IUX8MNB openfda.unii unii O3B55K4YKI openfda.unii unii 91D9GV0Z28 openfda.unii unii HF539G9L3Q openfda.unii unii 451W47IQ8X openfda.unii unii IHN2NQ5OF9 openfda.unii unii 2E32821G6I openfda.unii unii 3B8D35Y7S4 openfda.unii unii MA9CQJ3F7F openfda.unii unii E4GA8884NN openfda.unii unii 70WT22SF4B openfda.unii unii F5452U54PN 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: If pregnant or breastfeeding , ask a health professional before use. Do not use if clear seal over the cap is broken or missing. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away. Stop use and ask a doctor if fatigue, exhaustion, nervous irritability, muscle cramps, dizziness, or other symptoms do not improve within 7 days or are accompanied by fever.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.