United States · FDA National Drug Code directory

Anxiolix

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference: 61657-0006_b9708571-5b82-4644-e053-2995a90a6a12
Product NDC: 61657-0006
Form: LIQUID
Composition / generic term: ARSENICUM ALBUM ,SCUTELLARIA LATERIFLORA,PHOSPHORUS,LACHESIS MUTUS,PULSATILLA,PASSIFLORA INCARNATA,ACONITE,VALERIANA OFFICINALIS,CALCAREA CARBONICA,IGNATIA AMARA
Labeler: White Manufacturing Inc. DBA Micro West
Marketing category: UNAPPROVED HOMEOPATHIC
Marketing start / end (source format): 20110601
Source listing expiry: 20261231

Source-listed ingredients

ARSENIC TRIOXIDE — 12 [hp_X]/30mL
SCUTELLARIA LATERIFLORA — 3 [hp_X]/30mL
PHOSPHORUS — 12 [hp_X]/30mL
LACHESIS MUTA VENOM — 15 [hp_X]/30mL
PULSATILLA VULGARIS — 12 [hp_X]/30mL
PASSIFLORA INCARNATA FLOWERING TOP — 3 [hp_X]/30mL
ACONITUM NAPELLUS — 12 [hp_X]/30mL
VALERIAN — 3 [hp_X]/30mL
OYSTER SHELL CALCIUM CARBONATE, CRUDE — 12 [hp_X]/30mL
STRYCHNOS IGNATII SEED — 12 [hp_X]/30mL

These values do not establish equivalence or a dose recommendation.

Packages

30 mL in 1 BOTTLE, DROPPER (61657-0006-1) · 61657-0006-1

Source and coverage

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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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