FDA.reportPublic FDA data

Anxiolix

Manufacturer
White Manufacturing Inc. DBA Micro West
Effective date
2021-01-21
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
full-release
Hydrated at
2026-06-01 02:14:15

Label at a glance#

ProductAnxiolix
Active ingredientARSENIC TRIOXIDE, SCUTELLARIA LATERIFLORA, PHOSPHORUS, LACHESIS MUTA VENOM, PULSATILLA VULGARIS, PASSIFLORA INCARNATA FLOWERING TOP, ACONITUM NAPELLUS, VALERIAN, OYSTER SHELL CALCIUM CARBONATE, CRUDE, STRYCHNOS IGNATII SEED
Label structure10 sections

Dosage and administration

Directions: Take 6 drops orally, 4 times a day. For ages 2 to adult.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

Aconitum nap 12X

Arsenicum alb 12X

Calc carb 12X

Ignatia 12X

Lachesis 15X

Passiflora 3X

Phosphorus 12X

Pulsitilla 12X

Scutellaria 3X

Valeriana 3X

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Alcohol (2% v/v), Purified water

PURPOSE

OTC - PURPOSE SECTION

TEMPORARY RELIEF OF ANXIETY, SLEEPLESSNESS, NERVOUSNESS

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN

INDICATIONS

INDICATIONS & USAGE SECTION

INDICATIONS: FOR THE TEMPORARY RELIEF OF ANXIETY, SLEEPLESSNESS, NERVOUSNESS

WARNING

WARNINGS SECTION

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.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

Directions: Take 6 drops orally, 4 times a day. For ages 2 to adult.

MANUFACTURE

SPL UNCLASSIFIED SECTION

MANUFACTURED FOR

MICRO-WEST

DOUGLAS, WY 82633

1-307-358-5066

INACTIVE INGREDIENT SECTION

Alcohol (20%, v/v)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 61657-0006-1

MICRO-WEST

Homepathic

ANXIOLIX

Product #: 0006

1.0 fl oz bottle label1.0 fl oz bottle label

1.0 fl oz (29.6 mL)

Ethanol 20%

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
63f39a63-5cd1-4016-bd86-2bbb0f6c3139Product name320240506
e5a77e9c-c528-733a-173d-914a234c024bProduct name520240506

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
61657-0006-1Anxiolix30 mL in 1 BOTTLE, DROPPERLIQUID306

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
61657-0006ANXIOLIX (ARSENICUM ALBUM ,SCUTELLARIA LATERIFLORA,PHOSPHORUS,LACHESIS MUTUS,PULSATILLA,PASSIFLORA INCARNATA,ACONITE,VALERIANA OFFICINALIS,CALCAREA CARBONICA,IGNATIA AMARA) LIQUID [WHITE MANUFACTURING INC. DBA MICRO WEST]6Current NDC, Legacy NDC, 1 package rows20210123_69660f20-c9ba-4b43-bc85-0fab3ff68c61.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ACONITUM NAPELLUSACTIVE INGREDIENTU0NQ8555JD4
ARSENIC TRIOXIDEACTIVE INGREDIENTS7V92P67HO4
LACHESIS MUTA VENOMACTIVE INGREDIENTVSW71SS07I4
OYSTER SHELL CALCIUM CARBONATE, CRUDEACTIVE INGREDIENT2E32821G6I4
PASSIFLORA INCARNATA FLOWERING TOPACTIVE INGREDIENTCLF5YFS11O4
PHOSPHORUSACTIVE INGREDIENT27YLU75U4W4
PULSATILLA VULGARISACTIVE INGREDIENTI76KB35JEV4
SCUTELLARIA LATERIFLORAACTIVE INGREDIENT7BP4DH5PDC4
STRYCHNOS IGNATII SEEDACTIVE INGREDIENT1NM3M2487K4
VALERIANACTIVE INGREDIENTJWF5YAW3QW4
ACONITUM NAPELLUSACTIVE MOIETYU0NQ8555JD4
ARSENIC CATION (3+)ACTIVE MOIETYC96613F5AV4
LACHESIS MUTA VENOMACTIVE MOIETYVSW71SS07I4
OYSTER SHELL CALCIUM CARBONATE, CRUDEACTIVE MOIETY2E32821G6I4
PASSIFLORA INCARNATA FLOWERING TOPACTIVE MOIETYCLF5YFS11O4
PHOSPHORUSACTIVE MOIETY27YLU75U4W4
PULSATILLA VULGARISACTIVE MOIETYI76KB35JEV4
SCUTELLARIA LATERIFLORAACTIVE MOIETY7BP4DH5PDC4
STRYCHNOS IGNATII SEEDACTIVE MOIETY1NM3M2487K4
VALERIANACTIVE MOIETYJWF5YAW3QW4
ALCOHOLINACTIVE INGREDIENT3K9958V90M4

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
61657-000661657-0006-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MIACT
ARSENIC TRIOXIDES7V92P67HOACTIB
SCUTELLARIA LATERIFLORA7BP4DH5PDCACTIB
PHOSPHORUS27YLU75U4WACTIB
LACHESIS MUTA VENOMVSW71SS07IACTIB
PULSATILLA VULGARISI76KB35JEVACTIB
PASSIFLORA INCARNATA FLOWERING TOPCLF5YFS11OACTIB
ACONITUM NAPELLUSU0NQ8555JDACTIB
VALERIANJWF5YAW3QWACTIB
OYSTER SHELL CALCIUM CARBONATE, CRUDE2E32821G6IACTIB
STRYCHNOS IGNATII SEED1NM3M2487KACTIB

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 2 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
ALCOHOLALCOHOL3K9958V90MLIQUID / ORAL3563 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MLIQUID / ORAL3563 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
AnxiolixARSENICUM ALBUM ,SCUTELLARIA LATERIFLORA,PHOSPHORUS,LACHESIS MUTUS,PULSATILLA,PASSIFLORA INCARNATA,ACONITE,VALERIANA OFFICINALIS,CALCAREA CARBONICA,IGNATIA AMARAWhite Manufacturing Inc. DBA Micro West69660f20-c9ba-4b43-bc85-0fab3ff68c612021-01-21WarningsExact identifier
ndc (package): 61657-0006-1
ndc (product): 61657-0006
ndc11 (package): 61657000601
spl id: b9708571-5b82-4644-e053-2995a90a6a12
spl set id: 69660f20-c9ba-4b43-bc85-0fab3ff68c61

Reported adverse events (FAERS/openFDA)#

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