Easment Itch Defense Sulfur Cream

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: Easment Itch Defense Sulfur Cream
Generic name: SULFUR 1X HPUS
Manufacturer: Easment LLC
Product type: HUMAN OTC DRUG
SPL set ID: 4f140a93-dc32-0876-e063-6294a90a722a
SPL ID: 4f140a93-dc33-0876-e063-6294a90a722a
Version: 1
Effective date: 2026-04-09
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 05:15:08

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 · 9 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Easment Itch Defense Sulfur Cream	openfda.brand_name
generic name		SULFUR 1X HPUS	openfda.generic_name
manufacturer name		Easment LLC	openfda.manufacturer_name
ndc	package	87352-003-01	openfda.package_ndc
ndc	product	87352-003	openfda.product_ndc
ndc11	package	87352000301	derived:openfda.package_ndc
spl id		4f140a93-dc33-0876-e063-6294a90a722a	id
spl set id		4f140a93-dc32-0876-e063-6294a90a722a	set_id
unii		70FD1KFU70	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

For external use only. Ask a doctor before use if pregnant or nursing. When using this product, avoid contact with eyes, mouth, and mucous membranes. Stop use and ask a doctor if irritation, rash, or worsening symptoms occur, or if symptoms persist for more than 7 days. If swallowed, get medical help or contact a Poison Control Center right away at 1-800-222-1222.

Reported adverse events (FAERS/openFDA)#

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