Norms Hemorrhoid Wipes

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: Norms Hemorrhoid Wipes
Generic name: WITCH HAZEL
Manufacturer: Totally Normal Company
Product type: HUMAN OTC DRUG
SPL set ID: 5a1af50b-8d00-f589-e063-6394a90af86c
SPL ID: 5a1af572-0784-cd48-e063-6294a90ade91
Version: 1
Effective date: 2026-08-28
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 05:15:31

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 · 15 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M015	openfda.application_number
brand name		Norms Hemorrhoid Wipes	openfda.brand_name
generic name		WITCH HAZEL	openfda.generic_name
manufacturer name		Totally Normal Company	openfda.manufacturer_name
ndc	package	85996-002-03	openfda.package_ndc
ndc	package	85996-002-01	openfda.package_ndc
ndc	package	85996-002-02	openfda.package_ndc
ndc	product	85996-002	openfda.product_ndc
ndc11	package	85996000201	derived:openfda.package_ndc
ndc11	package	85996000202	derived:openfda.package_ndc
ndc11	package	85996000203	derived:openfda.package_ndc
rxcui		844379	openfda.rxcui
spl id		5a1af572-0784-cd48-e063-6294a90ade91	id
spl set id		5a1af50b-8d00-f589-e063-6394a90af86c	set_id
unii		101I4J0U34	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 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 7 days bleeding occurs If pregnant or breastfeeding ask a health professional before use.

Reported adverse events (FAERS/openFDA)#

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