Hypericum perforatum

Manufacturer
Boiron | Boiron, Inc.
Effective date
2025-12-30
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 02:36:31

Label at a glance#

ProductHypericum perforatum
Active ingredientHYPERICUM PERFORATUM
Label structure12 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient**(in each pellet)

Hypericum perforatum 30C HPUS (0.44 mg)

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*

Relieves nerve pain

INDICATIONS & USAGE SECTION

Uses*

temporarily relieves symptoms of nerve pain associated with minor injury such as:

  • radiating or shooting pain
  • pain in legs and back
  • toothaches

WARNINGS SECTION

Tube - (If using this product for toothache) For temporary use only until a dentist can be consulted.

OTC - STOP USE SECTION

Box - Stop use and ask a doctor if symptoms persist for more than 3 days or worsen, if new symptoms occur, or if redenss or swelling is present, as these could be signs of serious condition.

Tube - (If using this product for toothache) Stop use and ask a doctor if symptoms persist for more than 3 days or worsen, if new symptoms occur, or if redenss or swelling is present, as these could be signs of serious condition.

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

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

Tube - (If using this product for toothache) Keep out of reach of children. In case of accidental overdose, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

Adults and children: 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.

INACTIVE INGREDIENT SECTION

lactose, sucrose

OTC - QUESTIONS SECTION

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

BoironUSA.com Info@boiron.com
Distributed by Boiron, Inc. Newtown Square, PA 19073

SPL UNCLASSIFIED SECTION

Tube - Do not use if pellet dispenser seal is broken.
Contains approx 80 pellets.
How to dispense pellets? Turn tube upside down. Twist until 5 pellets are dispensed into cap. Carefully remove the cap and use it to 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.

Box - Do not use if glued carton end flaps are open or if pellet dispenser seal is broken.

3 Tubes approx 80 pellets 16 Doses per tube Total 240 pellets

1 Tube approx 80 pellets 16 Doses 80 pellets

How to dispense pellets? Turn tube upside down. Twist until 5 pellets are dispensed. Remove cap and pour pellets under the tongue.

Never Pain Relief*

Radiating or Shooting Pain*

*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

3030

303030c30c

LABELLABELLABELLABEL

LABELLABEL

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0220-2581-41Hypericum perforatum30 [hp_C] in 1 TUBEPELLET305
0220-2581-43Hypericum perforatum3 in 1 BOXPELLET35
0220-2581-43Hypericum perforatum30 [hp_C] in 1 TUBEPELLET305

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0220-25810220-2581-41, 0220-2581-43

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
Hypericum perforatumHYPERICUM PERFORATUMBoiron85ca8916-5b04-132e-e053-2a91aa0ac56d2025-12-30WarningsExact identifier
ndc (package): 0220-2581-41
ndc (package): 0220-2581-43
ndc (product): 0220-2581
ndc11 (package): 00220258143
ndc11 (package): 00220258141
spl id: 4730ade0-11f0-d7dc-e063-6394a90ad69f
spl set id: 85ca8916-5b04-132e-e053-2a91aa0ac56d

Reported adverse events (FAERS/openFDA)#

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