Anxiolix

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: Anxiolix
Generic name: ARSENICUM ALBUM ,SCUTELLARIA LATERIFLORA,PHOSPHORUS,LACHESIS MUTUS,PULSATILLA,PASSIFLORA INCARNATA,ACONITE,VALERIANA OFFICINALIS,CALCAREA CARBONICA,IGNATIA AMARA
Manufacturer: White Manufacturing Inc. DBA Micro West
Product type: HUMAN OTC DRUG
SPL set ID: 69660f20-c9ba-4b43-bc85-0fab3ff68c61
SPL ID: b9708571-5b82-4644-e053-2995a90a6a12
Version: 6
Effective date: 2021-01-21
Source export date: 2026-10-30
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/2026-10-30/023bc8d8aae5addb7530087bbbdb169b3ccbf36764f15b8ca67db07e1e5aea8b/drug-label-0008-of-0014.json.zip
Source manifest SHA-256: b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
Import run: 20261102T182004Z
Imported at: 2026-11-02 19:10:08

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 · 18 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Anxiolix	openfda.brand_name
generic name		ARSENICUM ALBUM ,SCUTELLARIA LATERIFLORA,PHOSPHORUS,LACHESIS MUTUS,PULSATILLA,PASSIFLORA INCARNATA,ACONITE,VALERIANA OFFICINALIS,CALCAREA CARBONICA,IGNATIA AMARA	openfda.generic_name
manufacturer name		White Manufacturing Inc. DBA Micro West	openfda.manufacturer_name
ndc	package	61657-0006-1	openfda.package_ndc
ndc	product	61657-0006	openfda.product_ndc
ndc11	package	61657000601	derived:openfda.package_ndc
spl id		b9708571-5b82-4644-e053-2995a90a6a12	id
spl set id		69660f20-c9ba-4b43-bc85-0fab3ff68c61	set_id
unii		27YLU75U4W	openfda.unii
unii		1NM3M2487K	openfda.unii
unii		2E32821G6I	openfda.unii
unii		S7V92P67HO	openfda.unii
unii		7BP4DH5PDC	openfda.unii
unii		JWF5YAW3QW	openfda.unii
unii		VSW71SS07I	openfda.unii
unii		U0NQ8555JD	openfda.unii
unii		CLF5YFS11O	openfda.unii
unii		I76KB35JEV	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 WARNING : 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.