CAND-EX

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: CAND-EX
Generic name: LYCOPODIUM,NUX VOMICA,BORAX,ASAFOETIDA,NUX MOSCHATA,GENTIANA LUTEA,KREOSOTUM,CALCAREA CARBONICA,SEPIA,PHOSPHORIC ACID,ECHINACEA,PULSATILLA,BAPTISIA,
Manufacturer: WHITE MANUFACTURING INC. DBA MICRO WEST
Product type: HUMAN OTC DRUG
SPL set ID: 4d650a1d-c6b5-410e-9e59-3753a373cc22
SPL ID: b97067fc-edb0-7e5d-e053-2a95a90afde5
Version: 6
Effective date: 2021-01-21
Source export date: 2026-09-28
Source partition: 6
Source file: https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:38:14

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 · 21 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		CAND-EX	openfda.brand_name
generic name		LYCOPODIUM,NUX VOMICA,BORAX,ASAFOETIDA,NUX MOSCHATA,GENTIANA LUTEA,KREOSOTUM,CALCAREA CARBONICA,SEPIA,PHOSPHORIC ACID,ECHINACEA,PULSATILLA,BAPTISIA,	openfda.generic_name
manufacturer name		WHITE MANUFACTURING INC. DBA MICRO WEST	openfda.manufacturer_name
ndc	package	61657-0101-1	openfda.package_ndc
ndc	product	61657-0101	openfda.product_ndc
ndc11	package	61657010101	derived:openfda.package_ndc
spl id		b97067fc-edb0-7e5d-e053-2a95a90afde5	id
spl set id		4d650a1d-c6b5-410e-9e59-3753a373cc22	set_id
unii		269XH13919	openfda.unii
unii		5K1UO2888Y	openfda.unii
unii		S72O3284MS	openfda.unii
unii		AEE24M3MQ9	openfda.unii
unii		91MBZ8H3QO	openfda.unii
unii		QDL83WN8C2	openfda.unii
unii		W9FZA51AS1	openfda.unii
unii		2E32821G6I	openfda.unii
unii		4N9P6CC1DX	openfda.unii
unii		E4GA8884NN	openfda.unii
unii		3JYG22FD73	openfda.unii
unii		I76KB35JEV	openfda.unii
unii		C88X29Y479	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 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.

Reported adverse events (FAERS/openFDA)#

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