Varicose Veins

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: Varicose Veins
Generic name: ELAPS CORALLINUS, CROTALUS HORRIDUS, BRYONIA, CALC. FLUOR., CARDUUS MAR., CHOLESTERINUM, CINCHONA, DIGITALIS, HAMAMELIS, HYDROFLUORICUM ACIDUM, LACHESIS, LYCOPODIUM, NAJA, PULSATILLA, VIPERA BERUS, ZINC. MET., AESCULUS HIPP., ECHINACEA
Manufacturer: Newton Laboratories, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 999b04b4-ffee-3532-e053-2a95a90a0662
SPL ID: b5e5161c-36d2-aa11-e053-2995a90a4241
Version: 2
Effective date: 2020-12-07
Source export date: 2026-09-28
Source partition: 6
Source file: https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:37:12

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 · 26 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Varicose Veins	openfda.brand_name
generic name		ELAPS CORALLINUS, CROTALUS HORRIDUS, BRYONIA, CALC. FLUOR., CARDUUS MAR., CHOLESTERINUM, CINCHONA, DIGITALIS, HAMAMELIS, HYDROFLUORICUM ACIDUM, LACHESIS, LYCOPODIUM, NAJA, PULSATILLA, VIPERA BERUS, ZINC. MET., AESCULUS HIPP., ECHINACEA	openfda.generic_name
manufacturer name		Newton Laboratories, Inc.	openfda.manufacturer_name
ndc	package	55714-4773-1	openfda.package_ndc
ndc	product	55714-4773	openfda.product_ndc
ndc11	package	55714477301	derived:openfda.package_ndc
spl id		b5e5161c-36d2-aa11-e053-2995a90a4241	id
spl set id		999b04b4-ffee-3532-e053-2a95a90a0662	set_id
unii		O3B55K4YKI	openfda.unii
unii		3C18L6RJAZ	openfda.unii
unii		U946SH95EE	openfda.unii
unii		RGL5YE86CZ	openfda.unii
unii		97C5T2UQ7J	openfda.unii
unii		0ORO6NCA4M	openfda.unii
unii		4N9P6CC1DX	openfda.unii
unii		S003A158SB	openfda.unii
unii		T7J046YI2B	openfda.unii
unii		V0S6H36980	openfda.unii
unii		VSW71SS07I	openfda.unii
unii		ZZ4AG7L7VM	openfda.unii
unii		F1T8QT9U8B	openfda.unii
unii		YHA2XLJ956	openfda.unii
unii		J41CSQ7QDS	openfda.unii
unii		I76KB35JEV	openfda.unii
unii		C88X29Y479	openfda.unii
unii		T7S323PKJS	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.