Naturium Sulfur Spot Treatment 8%

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: Naturium Sulfur Spot Treatment 8%
Generic name: SULFUR
Manufacturer: e.l.f. Cosmetics, Inc
Product type: HUMAN OTC DRUG
SPL set ID: 0a4a9aed-5eeb-f648-e063-6394a90a1d76
SPL ID: 43961b71-929a-943b-e063-6294a90afd73
Version: 3
Effective date: 2025-11-14
Source export date: 2026-09-28
Source partition: 13
Source file: https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/e78bf8aa9f90ab13e640d254dfbd4fe5bfeca4995ec5f9d51bce3356e249cab7/drug-label-0013-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:37:57

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		M006	openfda.application_number
brand name		Naturium Sulfur Spot Treatment 8%	openfda.brand_name
generic name		SULFUR	openfda.generic_name
manufacturer name		e.l.f. Cosmetics, Inc	openfda.manufacturer_name
ndc	package	76354-120-01	openfda.package_ndc
ndc	product	76354-120	openfda.product_ndc
ndc11	package	76354012001	derived:openfda.package_ndc
rxcui		2605592	openfda.rxcui
spl id		43961b71-929a-943b-e063-6294a90afd73	id
spl set id		0a4a9aed-5eeb-f648-e063-6394a90a1d76	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

Warnings For external use only. When using this product skin irritation and dryness is more likely to occur if you use another topical acne medication at the same time. If irritation occurs, only use one topical acne medication at a time. apply only to areas with acne Avoid eye area. In case of eye contact, flush gently and thoroughly with water. Do not use on broken skin large areas of the skin Keep out of reach of children.

Reported adverse events (FAERS/openFDA)#

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