Naturasil Mite B Gone

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: Naturasil Mite B Gone
Generic name: SULFUR, THUJA OCCIDENTALIS
Manufacturer: Nature's Innovation, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 79685f3a-9031-4bc5-9c1c-da0c7bbca967
SPL ID: 0bc5e84e-5b56-4656-a918-b270d3ee9c68
Version: 1
Effective date: 2025-11-07
Source export date: 2026-11-06
Source partition: 4
Source file: https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-11-06/b00a73f24c6ff050408c570063640e3d80d1f71dfc9a165d1cf072a25659445a/drug-label-0004-of-0014.json.zip
Source manifest SHA-256: 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run: 20261108T063105Z
Imported at: 2026-11-08 07:02:48

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 · 10 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Naturasil Mite B Gone	openfda.brand_name
generic name		SULFUR, THUJA OCCIDENTALIS	openfda.generic_name
manufacturer name		Nature's Innovation, Inc.	openfda.manufacturer_name
ndc	package	10893-661-05	openfda.package_ndc
ndc	product	10893-661	openfda.product_ndc
ndc11	package	10893066105	derived:openfda.package_ndc
spl id		0bc5e84e-5b56-4656-a918-b270d3ee9c68	id
spl set id		79685f3a-9031-4bc5-9c1c-da0c7bbca967	set_id
unii		0T0DQN8786	openfda.unii
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. Ask a doctor before use if pregnant or nursing. Avoid using near eyes, mouth or mucous membranes. If contact with eyes or mucous membranes occurs, rinse thoroughly with water. Keep out of reach of children. In case of ingestion, call Poison Control Center hotline immediately at 1-800-222-1222.

Reported adverse events (FAERS/openFDA)#

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