FDA.reportPublic FDA data

BMNP-LABEL COLCHICUM AUTUMNALE 30C

Manufacturer
Total Operations Management LLC DBA:Bestmade Natural Products Micro | BM Private Limited
Effective date
2026-09-25
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
daily-update
Hydrated at
2026-09-29 01:02:14

Label at a glance#

ProductBMNP COLCHICUM AUTUMNALE
Active ingredientCOLCHICUM AUTUMNALE BULB
Label structure8 sections

Label contents#

Full prescribing information#

WARNINGS SECTION

Keep out of reach of children.

If pregnant or breastfeeding, ask a health professional before use.

Stop use and ask a doctor if symptoms persist or worsen.

If you have severe symptoms, consult a doctor before use.

DOSAGE & ADMINISTRATION SECTION

Use as directed.

Take with water, 3-4 times daily. Ages 12 and older: 2 pellets. Ages 3 to 11: 1 pellet. Ages below 3: consult your doctor.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

If pregnant or breastfeeding, ask a health professional before use.

Stop use and ask a doctor if symptoms persist or worsen.

If you have severe symptoms, consult a doctor before use.

INDICATIONS & USAGE SECTION

Helps temporarily relieve: nausea from odors, digestive irritation, joint discomfort, abdominal sensitivity

OTC - PURPOSE SECTION

Colchicum Autumnale 30C (HPUS)......digestive upset, nausea, joint discomfort

"HPUS" is the Homeopathic Pharmacopoeia of the United States.

OTC - ACTIVE INGREDIENT SECTION

COLCHICUM AUTUMNALE 30C

INACTIVE INGREDIENT SECTION

Sucrose, PVP K 30, Magnesium Stearate, Aerosil

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Package 1

Colchicum Autumnale 30CColchicum Autumnale 30C

Package 2

Colchicum Aut 30CColchicum Aut 30C

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
QR code linkQR Codefastremedypicker.com/-_Colchicum Aut 30C.jpg

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82969-526482969-5264-1, 82969-5264-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
COLCHICUM AUTUMNALE BULB993QHL78E6ACTIB
MAGNESIUM STEARATE70097M6I30IACT
SUCROSEC151H8M554IACT
POVIDONE K30U725QWY32XIACT
SILICON DIOXIDEETJ7Z6XBU4IACT

Source Document#

Source XML

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 · 8 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Colchicum autumnaleCOLCHICUM AUTUMNALE BULBBoiron853e0580-d382-cda5-e053-2991aa0af3712023-11-09Name fallback
generic name: COLCHICUM AUTUMNALE BULB
Colchicum autumnaleCOLCHICUM AUTUMNALE BULBBoiron853ecad3-ad4e-32fe-e053-2991aa0ab96e2023-11-09Name fallback
generic name: COLCHICUM AUTUMNALE BULB
Colchicum autumnaleCOLCHICUM AUTUMNALE BULBBoiron853e3b67-acc0-3c15-e053-2a91aa0a64292023-11-09Name fallback
generic name: COLCHICUM AUTUMNALE BULB
Colchicum autumnaleCOLCHICUM AUTUMNALE BULBBoiron853dfd00-1afd-f471-e053-2a91aa0a015b2023-11-09Name fallback
generic name: COLCHICUM AUTUMNALE BULB
Colchicum autumnaleCOLCHICUM AUTUMNALE BULBBoiron853e9b51-6705-8564-e053-2991aa0a75472023-11-09Name fallback
generic name: COLCHICUM AUTUMNALE BULB
Colchicum autumnaleCOLCHICUM AUTUMNALE BULBBoiron34168f90-2a55-11e7-82ae-424c583030312023-11-09Name fallback
generic name: COLCHICUM AUTUMNALE BULB
Colchicum autumnaleCOLCHICUM AUTUMNALE BULBBoiron853e5860-d48c-b5d7-e053-2991aa0a4da72023-06-05Name fallback
generic name: COLCHICUM AUTUMNALE BULB
Colchicum autumnaleCOLCHICUM AUTUMNALE BULBBoiron853e7eee-c7a0-2b27-e053-2a91aa0a6a432023-02-20Name fallback
generic name: COLCHICUM AUTUMNALE BULB

Reported adverse events (FAERS/openFDA)#

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