Hemorrhoid Control Extra Strength

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: Hemorrhoid Control Extra Strength
Generic name: HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK AND HORSE CHESTNUT
Manufacturer: Forces of Nature
Product type: HUMAN OTC DRUG
SPL set ID: 868e373b-7404-4fd5-803b-4595035ee638
SPL ID: 4bda01fc-5b88-8b62-e063-6394a90aa6c8
Version: 5
Effective date: 2026-02-27
Source export date: 2026-09-28
Source partition: 10
Source file: https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/4bbc9760f647649b787710953d978bd6419e899ba8b90f32c3d972aae43947f8/drug-label-0010-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:06:13

Harmonized routes table
Harmonized routes
TOPICAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 16 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Hemorrhoid Control Extra Strength	openfda.brand_name
generic name		HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK AND HORSE CHESTNUT	openfda.generic_name
manufacturer name		Forces of Nature	openfda.manufacturer_name
ndc	package	51393-6447-3	openfda.package_ndc
ndc	package	51393-6447-2	openfda.package_ndc
ndc	package	51393-6447-1	openfda.package_ndc
ndc	package	51393-6447-5	openfda.package_ndc
ndc	product	51393-6447	openfda.product_ndc
ndc11	package	51393644701	derived:openfda.package_ndc
ndc11	package	51393644705	derived:openfda.package_ndc
ndc11	package	51393644703	derived:openfda.package_ndc
ndc11	package	51393644702	derived:openfda.package_ndc
spl id		4bda01fc-5b88-8b62-e063-6394a90aa6c8	id
spl set id		868e373b-7404-4fd5-803b-4595035ee638	set_id
unii		3C18L6RJAZ	openfda.unii
unii		T7S323PKJS	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings If pregnant or breast-feeding, ask a health professional before use. If accidental ingestion and adverse reaction occurs, get medical help or contact a Poison Control Center. For external use only. Some individuals may be sensitive to essential oils. Begin with a small drop to determine if product causes any irritation. Discontinue use if any irritation occurs. If condition worsens or does not improve, within 7 days, consult a doctor. Not for use on children under the age of 2 without physician direction. Keep out of reach of children.

Reported adverse events (FAERS/openFDA)#

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