R13 ADRENAL

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: R13 ADRENAL
Generic name: ACTIVATED CHARCOAL, CAUSTICUM, ARABICA COFFEE BEAN, PRASTERONE, GLYCYRRHIZA GLABRA, RIBES NIGRUM FLOWER BUD, ELEUTHERO, AND VERATRUM ALBUM ROOT
Manufacturer: Apex Energetics Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 2201816f-ddd6-4ef1-e063-6394a90aae4b
SPL ID: 2b36f19c-5632-f65d-e063-6394a90aa1fd
Version: 8
Effective date: 2025-01-08
Source export date: 2026-10-12
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/2026-10-12/fa098e7c5cff0b1ab653ce934059d1f4b90b860bafc0383a1f66223ce1037518/drug-label-0008-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 02:14:29

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 · 16 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		R13 ADRENAL	openfda.brand_name
generic name		ACTIVATED CHARCOAL, CAUSTICUM, ARABICA COFFEE BEAN, PRASTERONE, GLYCYRRHIZA GLABRA, RIBES NIGRUM FLOWER BUD, ELEUTHERO, AND VERATRUM ALBUM ROOT	openfda.generic_name
manufacturer name		Apex Energetics Inc.	openfda.manufacturer_name
ndc	package	63479-1813-2	openfda.package_ndc
ndc	product	63479-1813	openfda.product_ndc
ndc11	package	63479181302	derived:openfda.package_ndc
spl id		2b36f19c-5632-f65d-e063-6394a90aa1fd	id
spl set id		2201816f-ddd6-4ef1-e063-6394a90aae4b	set_id
unii		2P3VWU3H10	openfda.unii
unii		459AG36T1B	openfda.unii
unii		ZQH6VH092Z	openfda.unii
unii		2788Z9758H	openfda.unii
unii		3SW678MX72	openfda.unii
unii		DD5FO1WKFU	openfda.unii
unii		VYH9Y9BCCP	openfda.unii
unii		QNS6W5US1Z	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, stress, muscle weakness, dizziness when standing, hives, salt cravings, 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.