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#
Contacts and useful links#
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
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 0220-1492-41 | 2023-11-13 | C162847 | 48780-1 | f386c64a-3da8-0266-e053-dadaa90a7c1a | Collinsonia canadensis 8X |
| 0220-1492-41 | 2023-01-30 | C162847 | 48780-1 | f386c64a-3da8-0266-e053-dadaa90a7c1a | Collinsonia canadensis 8X |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 0220-1492-41 | Collinsonia canadensis | 8 [hp_X] in 1 TUBE | PELLET | 8 | 4 | |
| 0220-1492-43 | Collinsonia canadensis | 3 in 1 CARTON | PELLET | 3 | 4 |
Products#
Every source-derived product name is available through these pages.
- Collinsonia canadensis
- COLLINSONIA CANADENSIS ROOT
- SUCROSE
- LACTOSE, UNSPECIFIED FORM
- ANHYDROUS LACTOSE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 0220-1492 | 0220-1492-41, 0220-1492-43 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| SUCROSE | C151H8M554 | IACT |
| COLLINSONIA CANADENSIS ROOT | O2630F3XDR | ACTIB |
| LACTOSE, UNSPECIFIED FORM | J2B2A4N98G | IACT |
Source Document#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Collinsonia canadensis | COLLINSONIA CANADENSIS ROOT | Boiron | 6854bbd6-67e6-12c5-e053-2991aa0a1f7c | 2026-02-10 | 0220-1492-41 0220-1492-43 0220-1492 00220149241 00220149243 4a7cd2d7-2ef9-6e19-e063-6394a90a9326 6854bbd6-67e6-12c5-e053-2991aa0a1f7c |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.


