Earths Care Hemorrhoid Relief

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: Earths Care Hemorrhoid Relief
Generic name: WITCH HAZEL AND MENTHOL, UNSPECIFIED FORM
Manufacturer: DLC Laboratories, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: e860d65b-126d-4d77-8003-9d1381849ab5
SPL ID: 597f3fcb-f55d-3b9c-e063-6394a90aee23
Version: 8
Effective date: 2026-08-20
Source export date: 2026-10-12
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/2026-10-12/befa34274042a52f589b22fe2add0b1c6f0a385c96447c28303de164bb144af5/drug-label-0010-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 02:29:30

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 · 12 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M016	openfda.application_number
brand name		Earths Care Hemorrhoid Relief	openfda.brand_name
generic name		WITCH HAZEL AND MENTHOL, UNSPECIFIED FORM	openfda.generic_name
manufacturer name		DLC Laboratories, Inc.	openfda.manufacturer_name
ndc	package	24286-1570-1	openfda.package_ndc
ndc	product	24286-1570	openfda.product_ndc
ndc11	package	24286157001	derived:openfda.package_ndc
rxcui		2619742	openfda.rxcui
spl id		597f3fcb-f55d-3b9c-e063-6394a90aee23	id
spl set id		e860d65b-126d-4d77-8003-9d1381849ab5	set_id
unii		101I4J0U34	openfda.unii
unii		L7T10EIP3A	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 For external use only Allergy Alert Certain persons can develop allergic reactions to ingredients in this product When using this product do not exceed the recommended daily dosage unless directed by a doctor do not put this product into the rectum by using fingers or any mechanical device or applicator Stop use and ask a doctor if the symptom being treated does not subside or if redness, irritation, swelling, pain, or other symptoms develop or increase if bleeding occurs if condition worsens or does not improve within 7 days If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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