FDA.reportPublic FDA data

Hemorrhoid Relief

Manufacturer
King Bio Inc.
Effective date
2016-06-27
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:08:01

Label at a glance#

ProductHemorrhoid Relief
Active ingredientHORSE CHESTNUT, ALOE, COLLINSONIA CANADENSIS ROOT, HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK, HYDROCHLORIC ACID, STRYCHNOS NUX-VOMICA SEED, PAEONIA OFFICINALIS ROOT, KRAMERIA LAPPACEA ROOT, SEPIA OFFICINALIS JUICE, SULFUR
Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Drug Facts​__________________________________________________________________________________________________________

HPUS active ingredients: ​Aesculus hippocastanum, Aloe socotrina, Collinsonia canadensis, Hamamelis virginiana, Muriaticum acidum, Nux vomica, Paeonia officinalis, Ratanhia, Sepia, Sulphur. Equal volumes of each ingredient in 10X, 30X, LM1 potencies.

INDICATIONS & USAGE SECTION

Uses for temporary relief of hemorrhoid symptoms: burning or itching in anus, rectal pain, backache, constipation, blind or protruding hemorrhoids.

INACTIVE INGREDIENT SECTION

Inactive Ingredients:

Bio-Energetically Enhanced™ pure water, citric acid and potassium sorbate.

WARNINGS SECTION

Warnings

  • Stop use and ask your doctor if symptoms persist or worsen.
  • If pregnant or breast-feeding, ask a healthcare professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

  • Keep out of reach of children.

DOSAGE & ADMINISTRATION SECTION

Directions

  • Initially, depress pump until primed.
  • Spray one dose directly into mouth.
  • Ages 12 and up: 3 sprays 3 times per day.
  • Ages 2-12: 2 sprays 3 times per day.

OTHER SAFETY INFORMATION

Tamper resistant for your protection. Use only if safety seal is intact.

OTC - PURPOSE SECTION

Uses for temporary relief of hemorrhoid symptoms:

  • burning or itching in anus
  • rectal pain
  • backache
  • constipation
  • blind or protruding hemorrhoids

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
57955-5023-22020-01-31C16284748780-19d75b9d0-c505-f424-e053-dadaa90a57ceHemorrhoid Relief™

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
57955-5023-2Hemorrhoid Relief59 mL in 1 BOTTLE, SPRAYLIQUID591

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
57955-5023HEMORRHOID RELIEF (AESCULUS HIPPOCASTANUM, ALOE SOCOTRINA, COLLINSONIA CANADENSIS, HAMAMELIS VIRGINIANA, MURIATICUM ACIDUM, NUX VOMICA, PAEONIA OFFICINALIS, RATANHIA, SEPIA, SULPHUR) LIQUID [KING BIO INC.]1Legacy NDC, 1 package rows20160627_6ec9bbc5-ff37-4149-b4c9-b9cdf7af1dfa.zip

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
57955-502357955-5023-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
NameUNIIKind
HORSE CHESTNUT3C18L6RJAZACTIB
ALOEV5VD430YW9ACTIB
COLLINSONIA CANADENSIS ROOTO2630F3XDRACTIB
HAMAMELIS VIRGINIANA ROOT BARK/STEM BARKT7S323PKJSACTIB
HYDROCHLORIC ACIDQTT17582CBACTIB
STRYCHNOS NUX-VOMICA SEED269XH13919ACTIB
PAEONIA OFFICINALIS ROOT8R564U2E1PACTIB
KRAMERIA LAPPACEA ROOTP29ZH1A35ZACTIB
SEPIA OFFICINALIS JUICEQDL83WN8C2ACTIB
SULFUR70FD1KFU70ACTIB
ANHYDROUS CITRIC ACIDXF417D3PSLIACT
POTASSIUM SORBATE1VPU26JZZ4IACT
WATER059QF0KO0RIACT

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
9b0528be-28e5-48c7-b0bd-63b02de7b5fc6ec9bbc5-ff37-4149-b4c9-b9cdf7af1dfa2016-06-27WarningsExact identifier
spl id: 9b0528be-28e5-48c7-b0bd-63b02de7b5fc
spl set id: 6ec9bbc5-ff37-4149-b4c9-b9cdf7af1dfa

Reported adverse events (FAERS/openFDA)#

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