Doctor Butler Hemorrhoid and Fissure Advanced Formula

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: Doctor Butler Hemorrhoid and Fissure Advanced Formula
Generic name: GLYCERIN 37.5%, LANOLIN 12.5%, LIDOCAINE 4%, ZINC OXIDE 5%
Manufacturer: Beyond Health, PA
Product type: HUMAN OTC DRUG
SPL set ID: d2a769e2-afd0-aed2-e053-2995a90ad429
SPL ID: 3a9b3c55-04fb-8c74-e063-6294a90a0de8
Version: 5
Effective date: 2025-07-23
Source export date: 2026-09-28
Source partition: 2
Source file: https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:15:21

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 · 20 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M015	openfda.application_number
brand name		Doctor Butler Hemorrhoid and Fissure Advanced Formula	openfda.brand_name
generic name		GLYCERIN 37.5%, LANOLIN 12.5%, LIDOCAINE 4%, ZINC OXIDE 5%	openfda.generic_name
manufacturer name		Beyond Health, PA	openfda.manufacturer_name
ndc	package	70942-517-75	openfda.package_ndc
ndc	package	70942-517-07	openfda.package_ndc
ndc	package	70942-517-00	openfda.package_ndc
ndc	package	70942-517-01	openfda.package_ndc
ndc	product	70942-517	openfda.product_ndc
ndc11	package	70942051701	derived:openfda.package_ndc
ndc11	package	70942051707	derived:openfda.package_ndc
ndc11	package	70942051775	derived:openfda.package_ndc
ndc11	package	70942051700	derived:openfda.package_ndc
rxcui		2586855	openfda.rxcui
spl id		3a9b3c55-04fb-8c74-e063-6294a90a0de8	id
spl set id		d2a769e2-afd0-aed2-e053-2995a90ad429	set_id
unii		7EV65EAW6H	openfda.unii
unii		98PI200987	openfda.unii
unii		PDC6A3C0OX	openfda.unii
unii		SOI2LOH54Z	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 inclluding the skin of the anal canal 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 condition worsens or does not improve within seven (7) days bleeding occurs an allergic reaction develops the symptom being treated does not subside or if redness, irritation, swelling, pain or other symptoms develop or increase If pregnant or breast-feeding ask a health care professional before use. Keep out of reach of children If swallowed, seek 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.