Snore-Soothe

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: Snore-Soothe
Generic name: ECHINACEA, BRYONIA, CAMPHORA, CISTUS CANADENSIS, DROSERA, HEPAR SULPHURIS CALCAREUM, HYDRASTIS CANADENSIS, IGNATIA AMARA, IODIUM, KALI BICHROMICUM, KALI IODATUM, PHOSPHORUS, PULSATILLA, SABADILLA, SILICEA, STICTA PULMONARIA, SULPHUR, TEUCRIUM MARUM, VERBASCUM THAPSUS, ARSENICUM ALBUM, BELLADONNA, HISTAMINUM HYDROCHLORICUM, LAC CANINUM, NUX VOMICA
Manufacturer: Newton Laboratories, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 140a0bcf-82b3-c430-e063-6294a90ad38f
SPL ID: 140a19fd-51d7-c90b-e063-6394a90a1745
Version: 1
Effective date: 2024-03-19
Source export date: 2026-10-30
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/2026-10-30/e37bebe0ee356110e46fe9b102632217cd5fd64caa93a64cf6ef0d92a0bfdb4c/drug-label-0006-of-0014.json.zip
Source manifest SHA-256: b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
Import run: 20261102T182004Z
Imported at: 2026-11-02 18:51:42

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 · 32 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Snore-Soothe	openfda.brand_name
generic name		ECHINACEA, BRYONIA, CAMPHORA, CISTUS CANADENSIS, DROSERA, HEPAR SULPHURIS CALCAREUM, HYDRASTIS CANADENSIS, IGNATIA AMARA, IODIUM, KALI BICHROMICUM, KALI IODATUM, PHOSPHORUS, PULSATILLA, SABADILLA, SILICEA, STICTA PULMONARIA, SULPHUR, TEUCRIUM MARUM, VERBASCUM THAPSUS, ARSENICUM ALBUM, BELLADONNA, HISTAMINUM HYDROCHLORICUM, LAC CANINUM, NUX VOMICA	openfda.generic_name
manufacturer name		Newton Laboratories, Inc.	openfda.manufacturer_name
ndc	package	55714-2591-1	openfda.package_ndc
ndc	product	55714-2591	openfda.product_ndc
ndc11	package	55714259101	derived:openfda.package_ndc
spl id		140a19fd-51d7-c90b-e063-6394a90a1745	id
spl set id		140a0bcf-82b3-c430-e063-6294a90ad38f	set_id
unii		27YLU75U4W	openfda.unii
unii		269XH13919	openfda.unii
unii		3POA0Q644U	openfda.unii
unii		C9TD27U172	openfda.unii
unii		46G3W789Q3	openfda.unii
unii		G39P120JQT	openfda.unii
unii		9679TC07X4	openfda.unii
unii		ETJ7Z6XBU4	openfda.unii
unii		1NM3M2487K	openfda.unii
unii		S7V92P67HO	openfda.unii
unii		N20HL7Q941	openfda.unii
unii		4N9P6CC1DX	openfda.unii
unii		6NAF1689IO	openfda.unii
unii		ZW3Z11D0JV	openfda.unii
unii		WQZ3G9PF0H	openfda.unii
unii		T7J046YI2B	openfda.unii
unii		70FD1KFU70	openfda.unii
unii		1C4QK22F9J	openfda.unii
unii		T4423S18FM	openfda.unii
unii		J61BY05EGY	openfda.unii
unii		10464S0TAA	openfda.unii
unii		I76KB35JEV	openfda.unii
unii		D1YM0P5Z2T	openfda.unii
unii		1MBW07J51Q	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.