Female Femroids

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: Female Femroids
Generic name: HYDRASTIS CANADENSIS, THUJA OCCIDENTALIS, ARSENICUM ALBUM, CALCAREA IODATA, CARBO ANIMALIS, CONIUM MACULATUM, GRAPHITES, HYDRASTIS CANADENSIS, IODIUM, KREOSOTUM, LACHESIS MUTUS, PHOSPHORUS, SABINA, SECALE CORNUTUM, SEPIA, SILICEA, THLASPI BURSA-PASTORIS, THUJA OCCIDENTALIS, THYROIDINUM, TRILLIUM PENDULUM, USTILAGO MAIDIS.
Manufacturer: Newton Laboratories, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 9a01acb9-1b2b-3a33-e053-2995a90adc92
SPL ID: b592ade1-a61b-0588-e053-2995a90aa070
Version: 2
Effective date: 2020-12-03
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 · 27 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Female Femroids	openfda.brand_name
generic name		HYDRASTIS CANADENSIS, THUJA OCCIDENTALIS, ARSENICUM ALBUM, CALCAREA IODATA, CARBO ANIMALIS, CONIUM MACULATUM, GRAPHITES, HYDRASTIS CANADENSIS, IODIUM, KREOSOTUM, LACHESIS MUTUS, PHOSPHORUS, SABINA, SECALE CORNUTUM, SEPIA, SILICEA, THLASPI BURSA-PASTORIS, THUJA OCCIDENTALIS, THYROIDINUM, TRILLIUM PENDULUM, USTILAGO MAIDIS.	openfda.generic_name
manufacturer name		Newton Laboratories, Inc.	openfda.manufacturer_name
ndc	package	55714-4769-1	openfda.package_ndc
ndc	product	55714-4769	openfda.product_ndc
ndc11	package	55714476901	derived:openfda.package_ndc
spl id		b592ade1-a61b-0588-e053-2995a90aa070	id
spl set id		9a01acb9-1b2b-3a33-e053-2995a90adc92	set_id
unii		27YLU75U4W	openfda.unii
unii		4K7Z7K7SWG	openfda.unii
unii		0B4FDL9I6P	openfda.unii
unii		AHW6F0T2X0	openfda.unii
unii		4QQN74LH4O	openfda.unii
unii		Q28R5GF371	openfda.unii
unii		QDL83WN8C2	openfda.unii
unii		1NT28V9397	openfda.unii
unii		9679TC07X4	openfda.unii
unii		ETJ7Z6XBU4	openfda.unii
unii		W0X9457M59	openfda.unii
unii		S7V92P67HO	openfda.unii
unii		ZW3Z11D0JV	openfda.unii
unii		Z5BEX9K2G1	openfda.unii
unii		VSW71SS07I	openfda.unii
unii		3JYG22FD73	openfda.unii
unii		8EKI9QEE2H	openfda.unii
unii		279O8I0433	openfda.unii
unii		01G9XEA93N	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.