Vermafuge -AG Lycopodium

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: Vermafuge -AG Lycopodium
Generic name: NUX VOMICA,ARSENICUM ALBUM,CINCHONA OFFICINALIS,CAPSICUM ANNUUM,NITRIC ACID,MERCURIUSCORROSIVUS,BELLADONNA,CAJUPUTUM,LYCOPODIUM CLAVATUM,PHOSPHORUS,PHYTOLACCA DECANDRA,RHAMNUS PURSHIANA,FRAGARIA VESCA
Manufacturer: White Manufacturing Inc. DBA Micro-West
Product type: HUMAN OTC DRUG
SPL set ID: 447c7971-e7ea-4f47-82a2-ed6da883098f
SPL ID: b97044f4-0e78-5eb0-e053-2995a90a8021
Version: 5
Effective date: 2021-01-21
Source export date: 2026-09-28
Source partition: 2
Source file: https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:15:22

Harmonized routes table
Harmonized routes
ORAL

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 · 21 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Vermafuge -AG Lycopodium	openfda.brand_name
generic name		NUX VOMICA,ARSENICUM ALBUM,CINCHONA OFFICINALIS,CAPSICUM ANNUUM,NITRIC ACID,MERCURIUSCORROSIVUS,BELLADONNA,CAJUPUTUM,LYCOPODIUM CLAVATUM,PHOSPHORUS,PHYTOLACCA DECANDRA,RHAMNUS PURSHIANA,FRAGARIA VESCA	openfda.generic_name
manufacturer name		White Manufacturing Inc. DBA Micro-West	openfda.manufacturer_name
ndc	package	61657-1026-1	openfda.package_ndc
ndc	product	61657-1026	openfda.product_ndc
ndc11	package	61657102601	derived:openfda.package_ndc
spl id		b97044f4-0e78-5eb0-e053-2995a90a8021	id
spl set id		447c7971-e7ea-4f47-82a2-ed6da883098f	set_id
unii		27YLU75U4W	openfda.unii
unii		00UK7646FG	openfda.unii
unii		11E6VI8VEG	openfda.unii
unii		269XH13919	openfda.unii
unii		J3TO6BUQ37	openfda.unii
unii		411VRN1TV4	openfda.unii
unii		4VBP01X99F	openfda.unii
unii		53GH7MZT1R	openfda.unii
unii		S7V92P67HO	openfda.unii
unii		S003A158SB	openfda.unii
unii		WQZ3G9PF0H	openfda.unii
unii		CG6IX3GCMU	openfda.unii
unii		C88X29Y479	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

WARNING WARNINGS: STOP USE AND CALL A DOCTOR if symptoms persist or worsen. IF PREGNANT OR BREAST FEEDING, consult a healthcare professional before use. CONTAINS ALCOHOL: in case of accidental overdose, consult a poison control center immediately.

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.