F18 RLXTN

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: F18 RLXTN
Generic name: APRICOT, CHAMOMILE, COFFEA ARABICA, COFFEA CRUDA, COMFREY, CRIMSON MONKEY, DATE PALM, DILL, ENGLISH ELM ING TWIG, EUROPEAN ASPEN, FILAREE, GOLDEN EARDROPS, HORSE CHESTNUT, HUMULUS LUPULUS, HYPERICUM PERFORATUM, HYPERICUM PERFORATUM FLOWER, IMPATIENS GLANDULIFERA, MAGNESIA PHOSPHORICA, MEXICAN PINK, MIMULUS GUTTATUS, NUX VOMICA, OREGON GRAPEHOLLY, PASSIFLORA INCARNATA, SCUTELLARIA LATERIFLORA, SWEET CHESTNUT, VERBENA OFFICINALIS, WATERMELON, YERBA SANTA, ZINCUM VALERIANICUM
Manufacturer: Apex Energetics Inc.
Product type: HUMAN OTC DRUG
SPL set ID: bd1d02fd-9915-46d3-e053-2a95a90a39be
SPL ID: 0e77063c-fc3a-cee6-e063-6394a90a0d54
Version: 2
Effective date: 2024-01-08
Source export date: 2026-10-12
Source partition: 11
Source file: https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/a497e765d824a2e2aa9e88d5f0eea2aae9dcba363989e5f163395cda5c3c9dd8/drug-label-0011-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 02:44:49

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 · 38 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		F18 RLXTN	openfda.brand_name
generic name		APRICOT, CHAMOMILE, COFFEA ARABICA, COFFEA CRUDA, COMFREY, CRIMSON MONKEY, DATE PALM, DILL, ENGLISH ELM ING TWIG, EUROPEAN ASPEN, FILAREE, GOLDEN EARDROPS, HORSE CHESTNUT, HUMULUS LUPULUS, HYPERICUM PERFORATUM, HYPERICUM PERFORATUM FLOWER, IMPATIENS GLANDULIFERA, MAGNESIA PHOSPHORICA, MEXICAN PINK, MIMULUS GUTTATUS, NUX VOMICA, OREGON GRAPEHOLLY, PASSIFLORA INCARNATA, SCUTELLARIA LATERIFLORA, SWEET CHESTNUT, VERBENA OFFICINALIS, WATERMELON, YERBA SANTA, ZINCUM VALERIANICUM	openfda.generic_name
manufacturer name		Apex Energetics Inc.	openfda.manufacturer_name
ndc	package	63479-0618-1	openfda.package_ndc
ndc	product	63479-0618	openfda.product_ndc
ndc11	package	63479061801	derived:openfda.package_ndc
spl id		0e77063c-fc3a-cee6-e063-6394a90a0d54	id
spl set id		bd1d02fd-9915-46d3-e053-2a95a90a39be	set_id
unii		192426I5JU	openfda.unii
unii		MN0RX54EQA	openfda.unii
unii		XK4IUX8MNB	openfda.unii
unii		KK0Z92II8M	openfda.unii
unii		8QI9RWU9M1	openfda.unii
unii		269XH13919	openfda.unii
unii		3SW678MX72	openfda.unii
unii		5Q01F7TPJJ	openfda.unii
unii		HKE3DK7994	openfda.unii
unii		565ZR7YWT0	openfda.unii
unii		311PNK9CDZ	openfda.unii
unii		J4WG1JVR05	openfda.unii
unii		3VNC7T6Z02	openfda.unii
unii		4MGZ04S7LT	openfda.unii
unii		HF539G9L3Q	openfda.unii
unii		FJL3XFK3N8	openfda.unii
unii		AJU5O1A5ZV	openfda.unii
unii		68HKD4QMJR	openfda.unii
unii		J3O020I532	openfda.unii
unii		BWN6849791	openfda.unii
unii		7BP4DH5PDC	openfda.unii
unii		YHZ719F7M3	openfda.unii
unii		01G73H6H83	openfda.unii
unii		10TCS27K2T	openfda.unii
unii		231473QB6R	openfda.unii
unii		CLF5YFS11O	openfda.unii
unii		A6V4CUE7PV	openfda.unii
unii		90J8498ESR	openfda.unii
unii		H4ORZ75P00	openfda.unii
unii		H8FJJ6KX5Y	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 nervous irritability, exhaustion, worry, neck and back tension, 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.