Naturasil Scabies Relief

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 Scabies Relief
Generic name: SULFUR, THUJA OCCINDENTALIS
Manufacturer: Natures Innovation, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 6fa2c219-f0d4-43d5-a90c-75db471a8b5a
SPL ID: dd1faaa7-a019-4a21-9a6a-e20310c666d0
Version: 1
Effective date: 2020-10-22
Source export date: 2026-09-28
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/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:22:36

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 Scabies Relief	openfda.brand_name
generic name		SULFUR, THUJA OCCINDENTALIS	openfda.generic_name
manufacturer name		Natures Innovation, Inc.	openfda.manufacturer_name
ndc	package	10893-640-04	openfda.package_ndc
ndc	product	10893-640	openfda.product_ndc
ndc11	package	10893064004	derived:openfda.package_ndc
spl id		dd1faaa7-a019-4a21-9a6a-e20310c666d0	id
spl set id		6fa2c219-f0d4-43d5-a90c-75db471a8b5a	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.