Tobacco Withdrawal

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: Tobacco Withdrawal
Generic name: ARSENICUM ALB., BENZOICUM ACIDUM, BERBER. VULG., BRYONIA, CALADIUM SEGUINUM, CANTHARIS, CEANOTHUS, CHELIDONIUM MAJUS, CHIONANTHUS VIRGINICA, CINCHONA, DAPHNE INDICA, IGNATIA, IRIS VERSICOLOR, LYCOPODIUM, NICOTINUM, NUX VOM., RHUS TOXICODENDRON, SCUTELLARIA LATERIFLORA, TABACUM, ECHINACEA, TARAXACUM, VALERIANA
Manufacturer: Newton Laboratories, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 99eda7db-ce40-446f-e053-2995a90a95aa
SPL ID: b5e505a7-ca35-0d0a-e053-2a95a90ae77b
Version: 2
Effective date: 2020-12-07
Source export date: 2026-09-28
Source partition: 12
Source file: https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:28:08

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 · 29 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Tobacco Withdrawal	openfda.brand_name
generic name		ARSENICUM ALB., BENZOICUM ACIDUM, BERBER. VULG., BRYONIA, CALADIUM SEGUINUM, CANTHARIS, CEANOTHUS, CHELIDONIUM MAJUS, CHIONANTHUS VIRGINICA, CINCHONA, DAPHNE INDICA, IGNATIA, IRIS VERSICOLOR, LYCOPODIUM, NICOTINUM, NUX VOM., RHUS TOXICODENDRON, SCUTELLARIA LATERIFLORA, TABACUM, ECHINACEA, TARAXACUM, VALERIANA	openfda.generic_name
manufacturer name		Newton Laboratories, Inc.	openfda.manufacturer_name
ndc	package	55714-4732-1	openfda.package_ndc
ndc	product	55714-4732	openfda.product_ndc
ndc11	package	55714473201	derived:openfda.package_ndc
spl id		b5e505a7-ca35-0d0a-e053-2a95a90ae77b	id
spl set id		99eda7db-ce40-446f-e053-2995a90a95aa	set_id
unii		7E889U5RNN	openfda.unii
unii		269XH13919	openfda.unii
unii		JSJ34YQJ5D	openfda.unii
unii		8SKN0B0MIM	openfda.unii
unii		1TH8Q20J0U	openfda.unii
unii		39981FM375	openfda.unii
unii		6YR2608RSU	openfda.unii
unii		3Q034RO3BT	openfda.unii
unii		1NM3M2487K	openfda.unii
unii		6IO182RP7A	openfda.unii
unii		S7V92P67HO	openfda.unii
unii		4N9P6CC1DX	openfda.unii
unii		01800C6E6B	openfda.unii
unii		25B1Y14T8N	openfda.unii
unii		S003A158SB	openfda.unii
unii		7BP4DH5PDC	openfda.unii
unii		T7J046YI2B	openfda.unii
unii		JWF5YAW3QW	openfda.unii
unii		X43D4L3DQC	openfda.unii
unii		6M3C89ZY6R	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.