Hangover Help

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: Hangover Help
Generic name: AGARICUS MUSC., ARSENICUM ALB., BISMUTHUM METALLICUM, BRYONIA, CAPSICUM, CARBO VEG., GLONOINUM, IPECAC., IRIS VERSICOLOR, LAUROCERASUS, LYCOPODIUM, MEZEREUM, NUX VOM., PULSATILLA, RANUNC. BULB. , THERIDION, VERATRUM ALB., ZINC. MET., ZINGIBER, CHAMOMILLA, PASSIFLORA, VALERIANA
Manufacturer: Newton Laboratories, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 9bcce2ee-42c2-29cf-e053-2a95a90a3639
SPL ID: 2d81bd42-d226-4db0-e063-6294a90a7ba6
Version: 2
Effective date: 2025-02-06
Source export date: 2026-09-28
Source partition: 8
Source file: https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:55:51

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 · 30 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Hangover Help	openfda.brand_name
generic name		AGARICUS MUSC., ARSENICUM ALB., BISMUTHUM METALLICUM, BRYONIA, CAPSICUM, CARBO VEG., GLONOINUM, IPECAC., IRIS VERSICOLOR, LAUROCERASUS, LYCOPODIUM, MEZEREUM, NUX VOM., PULSATILLA, RANUNC. BULB. , THERIDION, VERATRUM ALB., ZINC. MET., ZINGIBER, CHAMOMILLA, PASSIFLORA, VALERIANA	openfda.generic_name
manufacturer name		Newton Laboratories, Inc.	openfda.manufacturer_name
ndc	package	55714-2450-1	openfda.package_ndc
ndc	product	55714-2450	openfda.product_ndc
ndc11	package	55714245001	derived:openfda.package_ndc
spl id		2d81bd42-d226-4db0-e063-6294a90a7ba6	id
spl set id		9bcce2ee-42c2-29cf-e053-2a95a90a3639	set_id
unii		2P3VWU3H10	openfda.unii
unii		00UK7646FG	openfda.unii
unii		269XH13919	openfda.unii
unii		X2N6E405GV	openfda.unii
unii		F26P2D4757	openfda.unii
unii		DIF093I037	openfda.unii
unii		U015TT5I8H	openfda.unii
unii		S7V92P67HO	openfda.unii
unii		AEQ8NXJ0MB	openfda.unii
unii		62I3C8233L	openfda.unii
unii		T7J046YI2B	openfda.unii
unii		JWF5YAW3QW	openfda.unii
unii		G59M7S0WS3	openfda.unii
unii		9Z8D3HEM8L	openfda.unii
unii		CLF5YFS11O	openfda.unii
unii		X43D4L3DQC	openfda.unii
unii		G0R4UBI2ZZ	openfda.unii
unii		J41CSQ7QDS	openfda.unii
unii		I76KB35JEV	openfda.unii
unii		QNS6W5US1Z	openfda.unii
unii		C5529G5JPQ	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.