Home FDA labels 0e77340b-340e-fe13-e063-6294a90a0301 N04 RAD-TOX 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 N04 RAD-TOX
Generic name ALOE SOCOTRINA, BONE MARROW SUIS, BOS TAURUS PLACENTA, BOS TAURUS SKIN, DNA, ECHINACEA ANGUSTIFOLIA, ECHINACEA PURPUREA, FERRUM METALLICUM, FUCUS VESICULOSUS, IODIUM, KALI PHOSPHORICUM, PHOSPHORUS, RIBES NIGRUM FLOWER BUD, SOY LECITHIN, VITAMIN A ACETATE, VITAMIN E ACETATE
Manufacturer Apex Energetics Inc.
Product type HUMAN OTC DRUG
SPL set ID bd08de24-ee4d-12bc-e053-2995a90a87b8
SPL ID 0e77340b-340e-fe13-e063-6294a90a0301
Version 2
Effective date 2024-01-08
Source export date 2026-09-28
Source partition 6
Source file https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 05:36:56 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 N04 RAD-TOX openfda.brand_name generic name ALOE SOCOTRINA, BONE MARROW SUIS, BOS TAURUS PLACENTA, BOS TAURUS SKIN, DNA, ECHINACEA ANGUSTIFOLIA, ECHINACEA PURPUREA, FERRUM METALLICUM, FUCUS VESICULOSUS, IODIUM, KALI PHOSPHORICUM, PHOSPHORUS, RIBES NIGRUM FLOWER BUD, SOY LECITHIN, VITAMIN A ACETATE, VITAMIN E ACETATE openfda.generic_name manufacturer name Apex Energetics Inc. openfda.manufacturer_name ndc package 63479-1404-1 openfda.package_ndc ndc product 63479-1404 openfda.product_ndc ndc11 package 63479140401 derived:openfda.package_ndc spl id 0e77340b-340e-fe13-e063-6294a90a0301 id spl set id bd08de24-ee4d-12bc-e053-2995a90a87b8 set_id unii 27YLU75U4W openfda.unii unii CI71S98N1Z openfda.unii unii 51FI676N6F openfda.unii unii VP2CN2G7Y8 openfda.unii unii 3LE3D9D6OY openfda.unii unii 9679TC07X4 openfda.unii unii VB06AV5US8 openfda.unii unii VYH9Y9BCCP openfda.unii unii V5VD430YW9 openfda.unii unii 535G2ABX9M openfda.unii unii QI7G114Y98 openfda.unii unii E1UOL152H7 openfda.unii unii 1DI56QDM62 openfda.unii unii 7J12CD6O9L openfda.unii unii 9E8X80D2L0 openfda.unii unii 83AL37E3A7 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 swelling, tiredness, exhaustion, weakness, nausea, 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.