Eye Care

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: Eye Care
Generic name: ACONITUM NAP., ALLIUM CEPA, ARSENICUM ALB., BRYONIA, CALENDULA, CHELIDONIUM MAJUS, CINERARIA, EUPHRASIA, GRAPHITES, LYCOPODIUM, MERC. CORROS., NUX VOM., PHOSPHORUS, PHYTOLACCA, PICRICUM AC., PULSATILLA, RHUS TOXICODENDRON, SULPHUR, ECHINACEA
Manufacturer: Newton Laboratories, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 924e562a-d9ae-5cae-e053-2995a90ace38
SPL ID: b4f4bf9f-d255-a951-e053-2a95a90ad028
Version: 2
Effective date: 2020-11-25
Source export date: 2026-09-28
Source partition: 10
Source file: https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/4bbc9760f647649b787710953d978bd6419e899ba8b90f32c3d972aae43947f8/drug-label-0010-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:08:23

Harmonized routes table
Harmonized routes
ORAL

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 · 27 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Eye Care	openfda.brand_name
generic name		ACONITUM NAP., ALLIUM CEPA, ARSENICUM ALB., BRYONIA, CALENDULA, CHELIDONIUM MAJUS, CINERARIA, EUPHRASIA, GRAPHITES, LYCOPODIUM, MERC. CORROS., NUX VOM., PHOSPHORUS, PHYTOLACCA, PICRICUM AC., PULSATILLA, RHUS TOXICODENDRON, SULPHUR, ECHINACEA	openfda.generic_name
manufacturer name		Newton Laboratories, Inc.	openfda.manufacturer_name
ndc	package	55714-2435-1	openfda.package_ndc
ndc	product	55714-2435	openfda.product_ndc
ndc11	package	55714243501	derived:openfda.package_ndc
spl id		b4f4bf9f-d255-a951-e053-2a95a90ad028	id
spl set id		924e562a-d9ae-5cae-e053-2995a90ace38	set_id
unii		27YLU75U4W	openfda.unii
unii		11E6VI8VEG	openfda.unii
unii		C9642I91WL	openfda.unii
unii		7E889U5RNN	openfda.unii
unii		269XH13919	openfda.unii
unii		4QQN74LH4O	openfda.unii
unii		18E7415PXQ	openfda.unii
unii		53GH7MZT1R	openfda.unii
unii		U4B223LS4X	openfda.unii
unii		6IO182RP7A	openfda.unii
unii		S7V92P67HO	openfda.unii
unii		4N9P6CC1DX	openfda.unii
unii		492225Q21H	openfda.unii
unii		T7J046YI2B	openfda.unii
unii		70FD1KFU70	openfda.unii
unii		U0NQ8555JD	openfda.unii
unii		A49OS0F91S	openfda.unii
unii		I76KB35JEV	openfda.unii
unii		C88X29Y479	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 SECTION WARNINGS: Keep out of reach of children. Do not use if tamper-evident seal is broken or missing. If symptoms worsen or persist for more than a few days, consult a doctor. If pregnant or breast-feeding , ask a doctor before use.

Reported adverse events (FAERS/openFDA)#

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