Thiosinaminum

Manufacturer: Washington Homeopathic Products
Effective date: 2025-01-28
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: full-release
Hydrated at: 2026-06-01 02:31:38

Label at a glance#

ProductThiosinaminum

Active ingredientALLYLTHIOUREA

Label structure8 sections

Indications and uses

Indicated for Scarring.

Dosage and administration

(Adults or Children): Dissolve 3 to 5 pellets under tongue 3 times a day or as directed by a licensed practitioner. Take at greater intervals as condition subsides.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

THIOSINAMINUM 200C

USES

OTC - PURPOSE SECTION

Indicated for Scarring.

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

As with all medications, keep out of reach of children.

INDICATIONS

INDICATIONS & USAGE SECTION

THIOSINAMINUM Scarring

STOP USE AND ASK DOCTOR

WARNINGS SECTION

If symptoms persist or recur, discontinue use. If pregnant or nursing, consult a licensed practitioner before using this product.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

(Adults or Children): Dissolve 3 to 5 pellets under tongue 3 times a day or as directed by a licensed practitioner. Take at greater intervals as condition subsides.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Sucrose/Lactose

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Thiosinaminum kit refill 200c

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
71919-820-01	Thiosinaminum	350 in 1 VIAL, GLASS	PELLET	350		3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
71919-820	THIOSINAMINUM (ALLYLTHIOUREA) PELLET [WASHINGTON HOMEOPATHIC PRODUCTS]	3	Current NDC, 1 package rows	20250130_09a6cc99-5ebd-5db7-e063-6294a90a80cf.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 4 matching rows.

Thiosinaminum
ALLYLTHIOUREA
SUCROSE
LACTOSE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
71919-820	71919-820-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
SUCROSE	C151H8M554	IACT
LACTOSE	J2B2A4N98G	IACT
ALLYLTHIOUREA	706IDJ14B7	ACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Thiosinaminum	ALLYLTHIOUREA	Washington Homeopathic Products	09a6cc99-5ebd-5db7-e063-6294a90a80cf	2025-01-28	Warnings	Exact identifier ndc (package): 71919-820-01 ndc (product): 71919-820 ndc11 (package): 71919082001 spl id: 2cc89b36-a4aa-6cac-e063-6394a90a524f spl set id: 09a6cc99-5ebd-5db7-e063-6294a90a80cf

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.