Major Medi-Pads

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: Major Medi-Pads
Generic name: WITCH HAZEL
Manufacturer: Major Pharmaceuticals
Product type: HUMAN OTC DRUG
SPL set ID: d2a314a2-98ab-4ac0-9e90-1a8c1303958f
SPL ID: 4539e5a6-0db0-02e3-e063-6294a90ad7a7
Version: 5
Effective date: 2025-12-05
Source export date: 2026-10-12
Source partition: 8
Source file: https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/fa098e7c5cff0b1ab653ce934059d1f4b90b860bafc0383a1f66223ce1037518/drug-label-0008-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 02:12:39

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 · 11 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M016	openfda.application_number
brand name		Major Medi-Pads	openfda.brand_name
generic name		WITCH HAZEL	openfda.generic_name
manufacturer name		Major Pharmaceuticals	openfda.manufacturer_name
ndc	package	0904-6829-60	openfda.package_ndc
ndc	product	0904-6829	openfda.product_ndc
ndc11	package	00904682960	derived:openfda.package_ndc
rxcui		844379	openfda.rxcui
spl id		4539e5a6-0db0-02e3-e063-6294a90ad7a7	id
spl set id		d2a314a2-98ab-4ac0-9e90-1a8c1303958f	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. 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 bleeding occurs condition worsens or does not improve within 7 days Keep out of reach of children If swallowed, get medical help or contact a Poison Control Center right away.(1-800-222-1222) If pregnant or breast-feeding ask a health professional before use.

Reported adverse events (FAERS/openFDA)#

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