Cataracc

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: Cataracc
Generic name: ARSENICUM ALB., BRYONIA, CALC. FLUOR., CALENDULA, CAUSTICUM, CONIUM, EUPHRASIA, HYDROFLUORICUM AC., IODIUM, LEDUM, NAPHTHALINUM, NAT. MUR., NUX VOM., PHOS., PULSATILLA, SEPIA, SILICEA, TELLURIUM, THIOSINAMINUM, ZINC. MET.
Manufacturer: Newton Laboratories, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: eff981fd-5436-7c34-e053-2a95a90a3e8e
SPL ID: eff981d9-abe5-a113-e053-2a95a90abfec
Version: 1
Effective date: 2022-12-16
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 05:26:32

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 · 28 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Cataracc	openfda.brand_name
generic name		ARSENICUM ALB., BRYONIA, CALC. FLUOR., CALENDULA, CAUSTICUM, CONIUM, EUPHRASIA, HYDROFLUORICUM AC., IODIUM, LEDUM, NAPHTHALINUM, NAT. MUR., NUX VOM., PHOS., PULSATILLA, SEPIA, SILICEA, TELLURIUM, THIOSINAMINUM, ZINC. MET.	openfda.generic_name
manufacturer name		Newton Laboratories, Inc.	openfda.manufacturer_name
ndc	package	55714-4847-1	openfda.package_ndc
ndc	product	55714-4847	openfda.product_ndc
ndc11	package	55714484701	derived:openfda.package_ndc
spl id		eff981d9-abe5-a113-e053-2a95a90abfec	id
spl set id		eff981fd-5436-7c34-e053-2a95a90a3e8e	set_id
unii		27YLU75U4W	openfda.unii
unii		877L01IZ0P	openfda.unii
unii		C9642I91WL	openfda.unii
unii		269XH13919	openfda.unii
unii		DD5FO1WKFU	openfda.unii
unii		O3B55K4YKI	openfda.unii
unii		2166IN72UN	openfda.unii
unii		Q28R5GF371	openfda.unii
unii		18E7415PXQ	openfda.unii
unii		QDL83WN8C2	openfda.unii
unii		9679TC07X4	openfda.unii
unii		ETJ7Z6XBU4	openfda.unii
unii		RGL5YE86CZ	openfda.unii
unii		451W47IQ8X	openfda.unii
unii		S7V92P67HO	openfda.unii
unii		T7J046YI2B	openfda.unii
unii		NQA0O090ZJ	openfda.unii
unii		706IDJ14B7	openfda.unii
unii		J41CSQ7QDS	openfda.unii
unii		I76KB35JEV	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.