dermveda SCABIES ITCH RELIEF SERUM

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: dermveda SCABIES ITCH RELIEF SERUM
Generic name: OLIVE EXTRACT, SULFUR
Manufacturer: Celcius Corp.
Product type: HUMAN OTC DRUG
SPL set ID: 86a8bffd-81a8-4f22-89b6-e51158f336db
SPL ID: e082640a-f278-42e7-b055-b13801a7ec8f
Version: 2
Effective date: 2026-02-09
Source export date: 2026-10-12
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/2026-10-12/b939c18fdf51df171cf60ce5558819d08ac66bb16bb9991d48cbec91028d783e/drug-label-0004-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 01:40:16

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		dermveda SCABIES ITCH RELIEF SERUM	openfda.brand_name
generic name		OLIVE EXTRACT, SULFUR	openfda.generic_name
manufacturer name		Celcius Corp.	openfda.manufacturer_name
ndc	package	83819-012-04	openfda.package_ndc
ndc	product	83819-012	openfda.product_ndc
ndc11	package	83819001204	derived:openfda.package_ndc
spl id		e082640a-f278-42e7-b055-b13801a7ec8f	id
spl set id		86a8bffd-81a8-4f22-89b6-e51158f336db	set_id
unii		MJ95C3OH47	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. Do not use • on children under 2 years of age unless directed by a doctor. • Avoid contact with eyes. When using this product • mild increase in irritation or burning may occur. Stop use and ask a doctor if • If symptoms persist or inflammation increases after 3 weeks of use or if the itch increases. • Increase in redness on skin. Pregnant or Breast Feeding • Ask a Health Professional before use. Keep out of reach of children . If swallowed, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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