FDA.reportPublic FDA data

RectiBiom Hemorrhoid Relief

Manufacturer
Biom Pharmaceutical Corporation
Effective date
2021-11-23
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 22:25:45

Label at a glance#

ProductRectiBiom Hemorrhoid Relief
Active ingredientAESCULUS HIPPOCASTANUM BARK, HAMAMELIS VIRGINIANA BARK, PAEONIA OFFICINALIS ROOT
Label structure8 sections

Indications and uses

• temporarily relieves symptomsof hemorrhoids such as: • burning • itching • swelling • pain • discomfort • helps shrink swollen hemorrhoids • relieves hemorrhoid symptoms following childbirth

Dosage and administration

Adults and children 12years of age and older: When practical, cleanse the affected area with milld soap and warm water and rinse thoroghly. Gently dry by patting or blotting with toilet tissue or a soft cloth before application of this product. Insert 1 suppository rectally morning and night. Children under 12 years of age: Ask a doctor

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

  • AESCULUS HIPPOCASTANUM - 7X HPUS (0.01g)
  • HAMAMELIS VIRGINIANA - 2X HPUS (0.01g)
  • PAEONIA OFFICINALIS ROOT - 2X HPUS (0.01g) 

Inactive Ingredients

INACTIVE INGREDIENT SECTION

  • HARD FAT
  • TURMERIC
  • CANDELILLA WAX
  • HYALURONIC ACID

Purpose

OTC - PURPOSE SECTION

  • Reduces swelling and relieves stinging pain associated with external hemorrhoids
  • Relieves burning,itching,and discomfort associated with hemorrhoids
  • Relieves burning pain and oozing associated with external hemorrhoids

Uses

INDICATIONS & USAGE SECTION

• temporarily relieves symptomsof hemorrhoids such as:
• burning • itching • swelling • pain • discomfort
• helps shrink swollen hemorrhoids
• relieves hemorrhoid symptoms following childbirth

Warnings

WARNINGS SECTION

For rectal use only.

Ask a doctor before use

OTC - ASK DOCTOR SECTION

in case of bleeding.

When using this product

OTC - WHEN USING SECTION

do not exceed the recommended daily dosage unless directed by a doctor.

Stop use and ask a doctor if

OTC - STOP USE SECTION

symptoms persist for more than 7 days or worsen.

If pregnant or breastfeeding

OTC - PREGNANCY OR BREAST FEEDING SECTION

ask a healthcare professional before use.

Keepout of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed,get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Adults and children 12years of age and older: When practical, cleanse the affected area with milld soap and warm water and rinse thoroghly. Gently dry by patting or blotting with toilet tissue or a soft cloth before application of this product. Insert 1 suppository rectally morning and night.
  • Children under 12 years of age: Ask a doctor

Other information

OTHER SAFETY INFORMATION

• Do not use if suppository seal is broken.
• Suppository shape and appearance will change when exposed to heat.
• Do not store above 8G°F (30°C)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Biom Pharmaceutical Corporation

Customer Information Center

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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
72959-00372959-003-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
AESCULUS HIPPOCASTANUM BARK7U76MXL14NACTIB
HAMAMELIS VIRGINIANA BARKIH3063S9MYACTIB
PAEONIA OFFICINALIS ROOT8R564U2E1PACTIB
HARD FAT8334LX7S21IACT
TURMERIC856YO1Z64FIACT
CANDELILLA WAXWL0328HX19IACT
HYALURONIC ACIDS270N0TRQYIACT

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
9358087d-a4a2-4cea-810d-c4cd3016bd69d614eadf-bef5-4713-9537-45efcdc5fbc32023-01-27WarningsExact identifier
spl set id: d614eadf-bef5-4713-9537-45efcdc5fbc3

Reported adverse events (FAERS/openFDA)#

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