dermveda NAIL FUNGUS 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 NAIL FUNGUS SERUM
Generic name: OLIVE EXTRACT, SULFUR
Manufacturer: Celcius Corp.
Product type: HUMAN OTC DRUG
SPL set ID: 6d999dac-7b84-4f19-957e-5c787a4e96c4
SPL ID: 41811716-a69c-4eeb-b613-64e1ef39adda
Version: 2
Effective date: 2026-02-09
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 05:14:58

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 NAIL FUNGUS SERUM	openfda.brand_name
generic name		OLIVE EXTRACT, SULFUR	openfda.generic_name
manufacturer name		Celcius Corp.	openfda.manufacturer_name
ndc	package	83819-120-04	openfda.package_ndc
ndc	product	83819-120	openfda.product_ndc
ndc11	package	83819012004	derived:openfda.package_ndc
spl id		41811716-a69c-4eeb-b613-64e1ef39adda	id
spl set id		6d999dac-7b84-4f19-957e-5c787a4e96c4	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 inflammation or burning may occur. Stop use and ask a doctor if • If symptoms persist or inflammation increases after 2 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.