Menstrual - PMS

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: Menstrual - PMS
Generic name: ANGELICA SINENSIS RADIX, ARSENICUM ALB., BRYONIA, CAULOPHYLLUM, CIMICIFUGA, CINCHONA, DIOSCOREA, FOLLICULINUM, GELSEMIUM, LACHESIS, LILIUM, LYCOPODIUM, MILLEFOLIUM, NUX VOM., PULSATILLA, SABINA, SECALE, SEPIA,THLASPI, VIBURNUM OP., ZINGIBER, ECHINACEA, VALERIANA
Manufacturer: Newton Laboratories, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 9c4a13c3-87ff-e833-e053-2995a90a8aba
SPL ID: 092fe390-ff03-13f2-e063-6394a90a5221
Version: 3
Effective date: 2023-11-02
Source export date: 2026-10-27
Source partition: 10
Source file: https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-27/eeb012fd0992efa4f76b2aef09dd5f84150b96392c46717c44deabcc4e3581c1/drug-label-0010-of-0014.json.zip
Source manifest SHA-256: 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run: 20261027T193451Z
Imported at: 2026-10-27 20:39:10

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 · 31 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Menstrual - PMS	openfda.brand_name
generic name		ANGELICA SINENSIS RADIX, ARSENICUM ALB., BRYONIA, CAULOPHYLLUM, CIMICIFUGA, CINCHONA, DIOSCOREA, FOLLICULINUM, GELSEMIUM, LACHESIS, LILIUM, LYCOPODIUM, MILLEFOLIUM, NUX VOM., PULSATILLA, SABINA, SECALE, SEPIA,THLASPI, VIBURNUM OP., ZINGIBER, ECHINACEA, VALERIANA	openfda.generic_name
manufacturer name		Newton Laboratories, Inc.	openfda.manufacturer_name
ndc	package	55714-2482-1	openfda.package_ndc
ndc	product	55714-2482	openfda.product_ndc
ndc11	package	55714248201	derived:openfda.package_ndc
spl id		092fe390-ff03-13f2-e063-6394a90a5221	id
spl set id		9c4a13c3-87ff-e833-e053-2995a90a8aba	set_id
unii		2FXJ6SW4PK	openfda.unii
unii		IWY3IWX2G8	openfda.unii
unii		269XH13919	openfda.unii
unii		T1UG6H6805	openfda.unii
unii		JTJ6HH6YEH	openfda.unii
unii		QDL83WN8C2	openfda.unii
unii		639KR60Q1Q	openfda.unii
unii		W0X9457M59	openfda.unii
unii		X67Z2963PI	openfda.unii
unii		S7V92P67HO	openfda.unii
unii		2DI9HA706A	openfda.unii
unii		4N9P6CC1DX	openfda.unii
unii		Z5BEX9K2G1	openfda.unii
unii		S003A158SB	openfda.unii
unii		T7J046YI2B	openfda.unii
unii		B66F4574UG	openfda.unii
unii		JWF5YAW3QW	openfda.unii
unii		VSW71SS07I	openfda.unii
unii		I76KB35JEV	openfda.unii
unii		01G9XEA93N	openfda.unii
unii		C5529G5JPQ	openfda.unii
unii		C88X29Y479	openfda.unii
unii		K73E24S6X9	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.