dermveda ULTRA EYE REMEDY

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 ULTRA EYE REMEDY
Generic name: SULPHUR, CURCUMA LONGA
Manufacturer: Celcius Corp.
Product type: HUMAN OTC DRUG
SPL set ID: 1088f138-dacb-4a7b-a623-c49e41bccb67
SPL ID: 00046bf1-58d5-438f-9c4f-10f9ab11f9c2
Version: 1
Effective date: 2026-03-18
Source export date: 2026-11-06
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/2026-11-06/245ea1c0d730b312e4410f082201cbe2cb4d1936fa2918316b6ea631293cbeba/drug-label-0013-of-0014.json.zip
Source manifest SHA-256: 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run: 20261108T063105Z
Imported at: 2026-11-08 08:10:44

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 ULTRA EYE REMEDY	openfda.brand_name
generic name		SULPHUR, CURCUMA LONGA	openfda.generic_name
manufacturer name		Celcius Corp.	openfda.manufacturer_name
ndc	package	83819-999-02	openfda.package_ndc
ndc	product	83819-999	openfda.product_ndc
ndc11	package	83819099902	derived:openfda.package_ndc
spl id		00046bf1-58d5-438f-9c4f-10f9ab11f9c2	id
spl set id		1088f138-dacb-4a7b-a623-c49e41bccb67	set_id
unii		856YO1Z64F	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 • Symptoms persist or inflammation increases after 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.