Advance Plus

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: Advance Plus
Generic name: CARDUUS MARIANUS, CYNARA SCOLYMUS, SOLIDAGO VIRGAUREA, TARAXACUM OFFICINALE, BENZOICUM ACIDUM, BERBERIS VULGARIS, BRYONIA (ALBA), CANTHARIS, CARDUUS BENEDICTUS, CEANOTHUS AMERICANUS, CHELIDONIUM MAJUS, CHIONANTHUS VIRGINICA, CINCHONA OFFICINALIS, DIOSCOREA VILLOSA, DOLICHOS PRURIENS, IRIS VERSICOLOR, JUNIPERUS COMMUNIS, NUX VOMICA, PTELEA TRIFOLIATA, URICUM ACIDUM
Manufacturer: VitaminMed, LLC
Product type: HUMAN OTC DRUG
SPL set ID: 97824fb3-e2b4-4807-943b-88e26b211bf1
SPL ID: 71920d36-a413-44e1-9e44-0342d3aea96f
Version: 4
Effective date: 2026-03-06
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 05:37:03

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		Advance Plus	openfda.brand_name
generic name		CARDUUS MARIANUS, CYNARA SCOLYMUS, SOLIDAGO VIRGAUREA, TARAXACUM OFFICINALE, BENZOICUM ACIDUM, BERBERIS VULGARIS, BRYONIA (ALBA), CANTHARIS, CARDUUS BENEDICTUS, CEANOTHUS AMERICANUS, CHELIDONIUM MAJUS, CHIONANTHUS VIRGINICA, CINCHONA OFFICINALIS, DIOSCOREA VILLOSA, DOLICHOS PRURIENS, IRIS VERSICOLOR, JUNIPERUS COMMUNIS, NUX VOMICA, PTELEA TRIFOLIATA, URICUM ACIDUM	openfda.generic_name
manufacturer name		VitaminMed, LLC	openfda.manufacturer_name
ndc	package	70964-0001-1	openfda.package_ndc
ndc	product	70964-0001	openfda.product_ndc
ndc11	package	70964000101	derived:openfda.package_ndc
spl id		71920d36-a413-44e1-9e44-0342d3aea96f	id
spl set id		97824fb3-e2b4-4807-943b-88e26b211bf1	set_id
unii		IWY3IWX2G8	openfda.unii
unii		268B43MJ25	openfda.unii
unii		3E271BSI0C	openfda.unii
unii		7E889U5RNN	openfda.unii
unii		269XH13919	openfda.unii
unii		5KQR6FTT0D	openfda.unii
unii		8SKN0B0MIM	openfda.unii
unii		1TH8Q20J0U	openfda.unii
unii		39981FM375	openfda.unii
unii		6L5ZL09795	openfda.unii
unii		U946SH95EE	openfda.unii
unii		3Q034RO3BT	openfda.unii
unii		25B1Y14T8N	openfda.unii
unii		S003A158SB	openfda.unii
unii		T7J046YI2B	openfda.unii
unii		O84B5194RL	openfda.unii
unii		5405K23S50	openfda.unii
unii		X43D4L3DQC	openfda.unii
unii		B71UA545DE	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: Stop use and ask a doctor if symptoms worsen or persist for more than a few days. If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away. Do not use if tamper evident seal is broken or missing. Keep tightly closed in a cool, dry place.

Reported adverse events (FAERS/openFDA)#

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