Collinsonia canadensis

Manufacturer
Boiron | Boiron Inc.
Effective date
2026-02-10
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 02:37:28

Label at a glance#

ProductCollinsonia canadensis
Active ingredientCOLLINSONIA CANADENSIS ROOT
Label structure12 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient** (in each pellet)

Collinsonia canadensis 8X HPUS (0.44 mg)

The letters “HPUS” indicate that the component in this product is officially monographed in the Homeopathic Pharmacopoeia of the United States.

OTC - PURPOSE SECTION

Collinsonia canadensis 8X HPUS (0.44 mg)………Relieves hemorrhoids associated with constipation

INDICATIONS & USAGE SECTION

Uses*

temporarily relieves symptoms of hemorrhoids associated with constipation such as:

  • burning
  • itching
  • pain
  • discomfort

OTC - ASK DOCTOR SECTION

Ask a doctor before use in case of bleeding.

OTC - STOP USE SECTION

Stop use and ask a doctor if symptoms persist for more than 3 days or worsen.

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding, ask a health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

  • Adults and children 12 years of age and older: At the onset of symptoms, dissolve 5 pellets under the tongue 3 times a day until symptoms are relieved or as directed by a doctor.
  • Children under 12 years of age: Ask a doctor.

INACTIVE INGREDIENT SECTION

lactose, sucrose

OTC - QUESTIONS SECTION

BoironUSA.com

Info@Boiron.com

1-800-BOIRON-1 (1-800-264-7661)

Made in France

Distributed by Boiron Inc.

Newtown Square, PA 19073

SPL UNCLASSIFIED SECTION

do not use if glued carton end flaps are open or if pellet dispenser seal is broken

contains 0.25 g of sugar per dose

retain carton for full drug facts

Constipation-Related

HEMORRHOID RELIEF*

Pain Itching Burning*

1 Tube

3 Tubes

APPROX. 80 PELLET EACH

TOTAL 240 PELLETS

Turn tube upside down

Twist until 5 pellets are dispensed

Remove cap and pour pellets under the tongue

*CLAIMS BASED ON TRADITIONAL HOMEOPATHIC PRACTICE, NOT ACCEPTED MEDICAL EVIDENCE. NOT FDA EVALUATED.
**C, K, CK, and X are homeopathic dilutions: see BoironUSA.com/info for details.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LABELLABEL

labellabellabellabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0220-1492-412023-11-13C16284748780-1f386c64a-3da8-0266-e053-dadaa90a7c1aCollinsonia canadensis 8X
0220-1492-412023-01-30C16284748780-1f386c64a-3da8-0266-e053-dadaa90a7c1aCollinsonia canadensis 8X

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0220-1492-41Collinsonia canadensis8 [hp_X] in 1 TUBEPELLET84
0220-1492-43Collinsonia canadensis3 in 1 CARTONPELLET34

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0220-14920220-1492-41, 0220-1492-43

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

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 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Collinsonia canadensisCOLLINSONIA CANADENSIS ROOTBoiron6854bbd6-67e6-12c5-e053-2991aa0a1f7c2026-02-10Exact identifier
ndc (package): 0220-1492-41
ndc (package): 0220-1492-43
ndc (product): 0220-1492
ndc11 (package): 00220149241
ndc11 (package): 00220149243
spl id: 4a7cd2d7-2ef9-6e19-e063-6394a90a9326
spl set id: 6854bbd6-67e6-12c5-e053-2991aa0a1f7c

Reported adverse events (FAERS/openFDA)#

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