Vermafuge -AG

Manufacturer
White Manufacturing Inc. DBA Micro-West
Effective date
2021-01-21
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 02:14:14

Label at a glance#

ProductVermafuge -AG Lycopodium
Active ingredientSTRYCHNOS NUX-VOMICA SEED, ARSENIC TRIOXIDE, CINCHONA OFFICINALIS BARK, CAPSICUM, NITRIC ACID, MERCURIC CHLORIDE, ATROPA BELLADONNA, CAJUPUT OIL, LYCOPODIUM CLAVATUM SPORE, PHOSPHORUS, PHYTOLACCA AMERICANA ROOT, FRANGULA PURSHIANA BARK, ALPINE STRAWBERRY
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

Arsenicum alb 12X

Belladonna 12X

Cajuputum 4X

Capsicum 3X

Cinchona 12X

Fragaria 12X

Lycopodium 12X

Merc corros 12X

Nitricum ac 12X

Nux vom 12X

Phos 12X

Phytolacca 6X

Rhamnus pursh 3X

PURPOSE

OTC - PURPOSE SECTION

FOR THE TEMPORARY RELIEF OF DYSENTERY, FLATULENCE, AND COLIC

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN

WARNING

WARNINGS SECTION

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.

OTHER SAFETY INFORMATION

OTHER INFORMATION: Tamper resistant for your protection. Use only if safety seal is intact.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

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

INDICATIONS

INDICATIONS & USAGE SECTION

INDICATIONS: FOR THE TEMPORARY RELIEF OF DYSENTARY, FLATULENCE, AND COLIC

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Alcohol 20% v/v

Purified water

MANUFACTURE

SPL UNCLASSIFIED SECTION

MANUFACTURED FOR

 MICRO-WEST

P.O. BOX 950

DOUGLAS, WY 82633

1-307-358-5066

LABEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 61657-1026-1

MICRO-WEST

Homeopathic

VERMAFUGE-AG

Product #: 1026

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
61657-1026-1Vermafuge -AGLycopodium30 mL in 1 BOTTLE, DROPPERLIQUID305

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
61657-1026VERMAFUGE -AG LYCOPODIUM (NUX VOMICA,ARSENICUM ALBUM,CINCHONA OFFICINALIS,CAPSICUM ANNUUM,NITRIC ACID,MERCURIUSCORROSIVUS,BELLADONNA,CAJUPUTUM,LYCOPODIUM CLAVATUM,PHOSPHORUS,PHYTOLACCA DECANDRA,RHAMNUS PURSHIANA,FRAGARIA VESCA) LIQUID [WHITE MANUFACTURING INC. DBA MICRO-WEST]5Current NDC, Legacy NDC, 1 package rows20210123_447c7971-e7ea-4f47-82a2-ed6da883098f.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ALPINE STRAWBERRYACTIVE INGREDIENTCG6IX3GCMU2
ARSENIC TRIOXIDEACTIVE INGREDIENTS7V92P67HO2
ATROPA BELLADONNAACTIVE INGREDIENTWQZ3G9PF0H2
CAJUPUT OILACTIVE INGREDIENTJ3TO6BUQ372
CAPSICUMACTIVE INGREDIENT00UK7646FG2
CINCHONA OFFICINALIS BARKACTIVE INGREDIENTS003A158SB2
FRANGULA PURSHIANA BARKACTIVE INGREDIENT4VBP01X99F2
LYCOPODIUM CLAVATUM SPOREACTIVE INGREDIENTC88X29Y4792
MERCURIC CHLORIDEACTIVE INGREDIENT53GH7MZT1R2
NITRIC ACIDACTIVE INGREDIENT411VRN1TV42
PHOSPHORUSACTIVE INGREDIENT27YLU75U4W2
PHYTOLACCA AMERICANA ROOTACTIVE INGREDIENT11E6VI8VEG2
STRYCHNOS NUX-VOMICA SEEDACTIVE INGREDIENT269XH139192
ALPINE STRAWBERRYACTIVE MOIETYCG6IX3GCMU2
ARSENIC CATION (3+)ACTIVE MOIETYC96613F5AV2
ATROPA BELLADONNAACTIVE MOIETYWQZ3G9PF0H2
CAJUPUT OILACTIVE MOIETYJ3TO6BUQ372
CAPSICUMACTIVE MOIETY00UK7646FG2
CINCHONA OFFICINALIS BARKACTIVE MOIETYS003A158SB2
FRANGULA PURSHIANA BARKACTIVE MOIETY4VBP01X99F2
LYCOPODIUM CLAVATUM SPOREACTIVE MOIETYC88X29Y4792
MERCURIC CATIONACTIVE MOIETYED30FJ8Y422
NITRIC ACIDACTIVE MOIETY411VRN1TV42
PHOSPHORUSACTIVE MOIETY27YLU75U4W2
PHYTOLACCA AMERICANA ROOTACTIVE MOIETY11E6VI8VEG2
STRYCHNOS NUX-VOMICA SEEDACTIVE MOIETY269XH139192
ALCOHOLINACTIVE INGREDIENT3K9958V90M2

Products#

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

DailyMed product names page 1 of 1 · 18 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
61657-102661657-1026-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

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
Vermafuge -AG LycopodiumNUX VOMICA,ARSENICUM ALBUM,CINCHONA OFFICINALIS,CAPSICUM ANNUUM,NITRIC ACID,MERCURIUSCORROSIVUS,BELLADONNA,CAJUPUTUM,LYCOPODIUM CLAVATUM,PHOSPHORUS,PHYTOLACCA DECANDRA,RHAMNUS PURSHIANA,FRAGARIA VESCAWhite Manufacturing Inc. DBA Micro-West447c7971-e7ea-4f47-82a2-ed6da883098f2021-01-21WarningsExact identifier
ndc (package): 61657-1026-1
ndc (product): 61657-1026
ndc11 (package): 61657102601
spl id: b97044f4-0e78-5eb0-e053-2995a90a8021
spl set id: 447c7971-e7ea-4f47-82a2-ed6da883098f

Reported adverse events (FAERS/openFDA)#

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