HEMCALM

Manufacturer
BOIRON | BOIRON, INC.
Effective date
2026-07-20
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
daily-update
Hydrated at
2026-07-23 05:10:02

Label at a glance#

ProductHEMCALM
Active ingredientHAMAMELIS VIRGINIANA ROOT BARK/STEM BARK, STRYCHNOS NUX-VOMICA SEED, HORSE CHESTNUT
Label structure12 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredients** (in each tablet)

Aesculus hippocastanum 6X HPUS (0.83 mg)

Hamamelis virginiana 6X HPUS (0.83 mg)

Nux vomica 12X HPUS (0.83 mg) (contains less than 10 -13 mg strychnine alkaloids)

The letters "HPUS" indicate that the components in this product are officially monographed in the Homeopathic Pharmacopoeia of the United States.

OTC - PURPOSE SECTION

Purpose*

Aesculus hippocastanum 6X HPUS (0.83 mg) ... Reduces swelling and relieves stinging pain associated with internal and external hemorrhoids

Hamamelis virginiana 6X HPUS (0.83 mg) ... Relieves burning, itching, and discomfort associated with hemorrhoids

Nux vomica 12X HPUS (0.83 mg) ... Relieves painful hemorrhoids associated with overeating and sedentary lifestyles

INDICATIONS & USAGE SECTION

Uses *

temporarily relieves symptoms of hemorrhoids such as:

  • burning
  • itching
  • swelling
  • pain
  • discomfort
  • temporarily shrinks hemorrhoidal tissue
  • relieves hemorrhoid symptoms following childbirth

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 7 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 2 tablets in the mouth every 2 hours, up to 6 times a day.

Children under 12 years of age: Ask a doctor.

SPL UNCLASSIFIED SECTION

do not use if glued carton end flaps are open or if the blister seal is broken

store below 86° F (30° C)

60 MELTAWAY TABLETS Unflavored

100 MELTAWAY TABLETS Unflavored

Hemorrhoid Relief*

Burning, Itching, Pain, Discomfort*

Relieves Internal & External Hemorrhoids*

Plant-Powered Relief

No known drug interactions

Suitable for hemorrhoids following childbirth*

Made in France

Distributed by Boiron, Inc. Newtown Square, PA 19073

*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.

INACTIVE INGREDIENT SECTION

croscarmellose sodium, lactose, magnesium stearate

OTC - QUESTIONS SECTION

1-800-BOIRON-1 (1-800-264-7661)
BoironUSA.com Info@boiron.com

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0220-9180-042023-06-13C16284748780-1f386c64a-4145-0266-e053-dadaa90a7c1aHEMCALM
0220-9180-042023-06-13C16284748780-1f386c64a-4145-0266-e053-dadaa90a7c1aHEMCALM
0220-9180-042023-01-30C16284748780-1f386c64a-4145-0266-e053-dadaa90a7c1aHEMCALM
0220-9180-042023-01-30C16284748780-1f386c64a-4145-0266-e053-dadaa90a7c1aHEMCALM

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0220-91800220-9180-04, 0220-9180-92

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
52024-02-08full-release2026-06-01 02:26:02

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
HEMCALMHORSE CHESTNUT, HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK, STRYCHNOS NUX-VOMICA SEEDBOIRON8f8c295f-b6ec-6c6f-e053-2995a90aad9e2026-07-20Exact identifier
ndc (package): 0220-9180-04
ndc (package): 0220-9180-92
ndc (product): 0220-9180
ndc11 (package): 00220918004
ndc11 (package): 00220918092
spl id: 570dd46a-8553-d130-e063-6294a90a96ee
spl set id: 8f8c295f-b6ec-6c6f-e053-2995a90aad9e

Reported adverse events (FAERS/openFDA)#

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