F10 WRMLV

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: F10 WRMLV
Generic name: AGRIMONY, ALOE VERA, AURUM METALLICUM, AZURITE, BASIL, CALENDULA OFFICINALIS, CARICA PAPAYA, CAYENNE, DAFFODIL, DICENTRA FORMOSA, DIPLACUS AURANTIACUS, HIBISCUS CHINENSIS, HORSE CHESTNUT, HYLOTELEPHIUM TELEPHIUM, LAVANDULA STOECHAS, LILIUM TIGRINUM, MALVA NEGLECTA, MELILOTUS ALBA, NELUMBO NUCIFERA, PHOSPHORUS, PRUNELLA VULGARIS, ROSA LUCIAE, ROSEMARY, SCUTELLARIA LATERIFLORA, SEPIA, SILICEA, THUJA OCCIDENTALIS, TOXICODENDRON DIVERSILOBUM, VIOLA ODORATA, YELLOW JASMINE
Manufacturer: Apex Energetics Inc.
Product type: HUMAN OTC DRUG
SPL set ID: bf020c17-578d-74c4-e053-2995a90a9e7d
SPL ID: 0e76f0d9-0ac8-e097-e063-6394a90adba2
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 05:55:52

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		F10 WRMLV	openfda.brand_name
generic name		AGRIMONY, ALOE VERA, AURUM METALLICUM, AZURITE, BASIL, CALENDULA OFFICINALIS, CARICA PAPAYA, CAYENNE, DAFFODIL, DICENTRA FORMOSA, DIPLACUS AURANTIACUS, HIBISCUS CHINENSIS, HORSE CHESTNUT, HYLOTELEPHIUM TELEPHIUM, LAVANDULA STOECHAS, LILIUM TIGRINUM, MALVA NEGLECTA, MELILOTUS ALBA, NELUMBO NUCIFERA, PHOSPHORUS, PRUNELLA VULGARIS, ROSA LUCIAE, ROSEMARY, SCUTELLARIA LATERIFLORA, SEPIA, SILICEA, THUJA OCCIDENTALIS, TOXICODENDRON DIVERSILOBUM, VIOLA ODORATA, YELLOW JASMINE	openfda.generic_name
manufacturer name		Apex Energetics Inc.	openfda.manufacturer_name
ndc	package	63479-0610-1	openfda.package_ndc
ndc	product	63479-0610	openfda.product_ndc
ndc11	package	63479061001	derived:openfda.package_ndc
spl id		0e76f0d9-0ac8-e097-e063-6394a90adba2	id
spl set id		bf020c17-578d-74c4-e053-2995a90a9e7d	set_id
unii		27YLU75U4W	openfda.unii
unii		S0QQA41760	openfda.unii
unii		00UK7646FG	openfda.unii
unii		0PMA62ZZ6X	openfda.unii
unii		5811MI029U	openfda.unii
unii		KK0Z92II8M	openfda.unii
unii		6OFG7K362R	openfda.unii
unii		AT1FD041EF	openfda.unii
unii		7SAB275FP2	openfda.unii
unii		18E7415PXQ	openfda.unii
unii		QDL83WN8C2	openfda.unii
unii		NR1A27F29O	openfda.unii
unii		9211E5735B	openfda.unii
unii		70759G2U6A	openfda.unii
unii		1NT28V9397	openfda.unii
unii		639KR60Q1Q	openfda.unii
unii		575DY8C1ER	openfda.unii
unii		ETJ7Z6XBU4	openfda.unii
unii		79Y1949PYO	openfda.unii
unii		X67Z2963PI	openfda.unii
unii		599O6K8K81	openfda.unii
unii		61W322NLDV	openfda.unii
unii		9AD6E582QL	openfda.unii
unii		S0U63B0Q51	openfda.unii
unii		C6CNB75R61	openfda.unii
unii		438W01FC7A	openfda.unii
unii		L879RBF1WN	openfda.unii
unii		TO6G4140YA	openfda.unii
unii		PH797NEU5T	openfda.unii
unii		123T84GFBH	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 desire for solitiude, great indifference, sadness, drowsiness, sighing, fear, 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.