FDA.reportPublic FDA data

CAND-EX

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 02:14:14

Label at a glance#

ProductCAND-EX
Active ingredientLYCOPODIUM CLAVATUM SPORE, STRYCHNOS NUX-VOMICA SEED, ECHINACEA, UNSPECIFIED, BAPTISIA TINCTORIA, PULSATILLA VULGARIS, SEPIA OFFICINALIS JUICE, PHOSPHORIC ACID, WOOD CREOSOTE, OYSTER SHELL CALCIUM CARBONATE, CRUDE, SODIUM BORATE, GENTIANA LUTEA ROOT, NUTMEG, ASAFETIDA
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

Asafoetida 12X

Baptisia 3X

Borax 12X

Calc carb 12X

Echinacea 3X

Gentiana lut 3X

Kreosotum 12X

Lycopodium 30X

Nux mosch 12X

Nux vom 12X

Phosphoricum ac 12X

Pulsatilla 30X

Sepia 30X

Inactive ingredients

INACTIVE INGREDIENT SECTION

Inactive ingredients: Alcohol (20% v/v), Purified water

PURPOSE

OTC - PURPOSE SECTION

FOR THE TEMPORARY RELIEF OF FLATULENCE, DROWSINESS, CONFUSION, VERITGO, HEADACHE, NAUSEA, AND VAGINAL DISCHARGE

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 FLATULENCE, DROWSINESS, CONFUSION, VERITGO, HEADACHE, NAUSEA, AND VAGINAL DISCHARGE

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.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

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

Other Information

OTHER SAFETY INFORMATION

Other information: Tamper resistant for your protection. Use only if safety seal is intact

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 61657-0101-1

MICRO-WEST

Homeopathic

CAND-EX

Product #: 0101

1.0 fl oz Bottle Label1.0 fl oz Bottle Label

1.0  fl oz (29.6 mL)

Ethanol 20%

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
61657-0101-1CAND-EX30 mL in 1 BOTTLE, DROPPERLIQUID306

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
61657-0101CAND-EX (LYCOPODIUM,NUX VOMICA,BORAX,ASAFOETIDA,NUX MOSCHATA,GENTIANA LUTEA,KREOSOTUM,CALCAREA CARBONICA,SEPIA,PHOSPHORIC ACID,ECHINACEA,PULSATILLA,BAPTISIA,) LIQUID [WHITE MANUFACTURING INC. DBA MICRO WEST]6Current NDC, Legacy NDC, 1 package rows20210123_4d650a1d-c6b5-410e-9e59-3753a373cc22.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ASAFETIDAACTIVE INGREDIENTW9FZA51AS14
BAPTISIA TINCTORIAACTIVE INGREDIENT5K1UO2888Y4
ECHINACEA, UNSPECIFIEDACTIVE INGREDIENT4N9P6CC1DX4
GENTIANA LUTEA ROOTACTIVE INGREDIENTS72O3284MS4
LYCOPODIUM CLAVATUM SPOREACTIVE INGREDIENTC88X29Y4794
NUTMEGACTIVE INGREDIENTAEE24M3MQ94
OYSTER SHELL CALCIUM CARBONATE, CRUDEACTIVE INGREDIENT2E32821G6I4
PHOSPHORIC ACIDACTIVE INGREDIENTE4GA8884NN4
PULSATILLA VULGARISACTIVE INGREDIENTI76KB35JEV4
SEPIA OFFICINALIS JUICEACTIVE INGREDIENTQDL83WN8C24
SODIUM BORATEACTIVE INGREDIENT91MBZ8H3QO4
STRYCHNOS NUX-VOMICA SEEDACTIVE INGREDIENT269XH139194
WOOD CREOSOTEACTIVE INGREDIENT3JYG22FD734
ASAFETIDAACTIVE MOIETYW9FZA51AS14
BAPTISIA TINCTORIAACTIVE MOIETY5K1UO2888Y4
BORATE IONACTIVE MOIETY44OAE30D224
ECHINACEA, UNSPECIFIEDACTIVE MOIETY4N9P6CC1DX4
GENTIANA LUTEA ROOTACTIVE MOIETYS72O3284MS4
LYCOPODIUM CLAVATUM SPOREACTIVE MOIETYC88X29Y4794
NUTMEGACTIVE MOIETYAEE24M3MQ94
OYSTER SHELL CALCIUM CARBONATE, CRUDEACTIVE MOIETY2E32821G6I4
PHOSPHORIC ACIDACTIVE MOIETYE4GA8884NN4
PULSATILLA VULGARISACTIVE MOIETYI76KB35JEV4
SEPIA OFFICINALIS JUICEACTIVE MOIETYQDL83WN8C24
STRYCHNOS NUX-VOMICA SEEDACTIVE MOIETY269XH139194
WOOD CREOSOTEACTIVE MOIETY3JYG22FD734
ALCOHOLINACTIVE INGREDIENT3K9958V90M4

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
61657-010161657-0101-1

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MIACT
LYCOPODIUM CLAVATUM SPOREC88X29Y479ACTIB
STRYCHNOS NUX-VOMICA SEED269XH13919ACTIB
ECHINACEA, UNSPECIFIED4N9P6CC1DXACTIB
BAPTISIA TINCTORIA5K1UO2888YACTIB
PULSATILLA VULGARISI76KB35JEVACTIB
SEPIA OFFICINALIS JUICEQDL83WN8C2ACTIB
PHOSPHORIC ACIDE4GA8884NNACTIB
WOOD CREOSOTE3JYG22FD73ACTIB
OYSTER SHELL CALCIUM CARBONATE, CRUDE2E32821G6IACTIB
SODIUM BORATE91MBZ8H3QOACTIB
GENTIANA LUTEA ROOTS72O3284MSACTIB
NUTMEGAEE24M3MQ9ACTIB
ASAFETIDAW9FZA51AS1ACTIB

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
CAND-EXLYCOPODIUM,NUX VOMICA,BORAX,ASAFOETIDA,NUX MOSCHATA,GENTIANA LUTEA,KREOSOTUM,CALCAREA CARBONICA,SEPIA,PHOSPHORIC ACID,ECHINACEA,PULSATILLA,BAPTISIA,WHITE MANUFACTURING INC. DBA MICRO WEST4d650a1d-c6b5-410e-9e59-3753a373cc222021-01-21WarningsExact identifier
ndc (package): 61657-0101-1
ndc (product): 61657-0101
ndc11 (package): 61657010101
spl id: b97067fc-edb0-7e5d-e053-2a95a90afde5
spl set id: 4d650a1d-c6b5-410e-9e59-3753a373cc22

Reported adverse events (FAERS/openFDA)#

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