FDA.reportPublic FDA data

Scab Ease Itch Relief

Manufacturer
Feelgood Health | W. Last
Effective date
2010-07-28
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 02:02:30

Label at a glance#

ProductScab Ease Itch Relief
Active ingredientSCABIES LESION LYSATE (HUMAN), DELPHINIUM STAPHISAGRIA SEED, VIOLA TRICOLOR
Label structure11 sections

Label contents#

Full prescribing information#

OTC - PURPOSE SECTION

Relieves intense itching and nocturnal discomfort

INDICATIONS & USAGE SECTION

Indications: Homeopathic remedy for the relief of itching and irritation.

DOSAGE & ADMINISTRATION SECTION

Dosage: Mix 10 drops in ¼ cup water and sip slowly. Repeat 3-5 times daily as needed until symptoms subside. If preferred, drops may be taken directly into the mouth. Children under 12: Reduce dosage to 5 drops, 3-5 times daily. May be used with Itch Dr.™ cream.

GENERAL PRECAUTIONS SECTION

Caution: Consult your doctor if symptoms persist or worsen. Keep this and all medicines out of reach of children.

OTC - ACTIVE INGREDIENT SECTION

Ingredients: Each dose contains equal parts of Psorinum (12C) (HPUS), Staphisagria (12C) (HPUS), Viola tri (12C) (HPUS)

INACTIVE INGREDIENT SECTION

Citricidal extract (inactive ingredient).

PREGNANCY SECTION

If pregnant or breastfeeding, ask a health professional before use.

WARNINGS SECTION

Contains no animal products, gluten, artificial flavors, preservatives, colorants or alcohol. Suitable for vegetarians and safe for all ages.

INFORMATION FOR PATIENTS SECTION

All Native Remedies health products are especially formulated by experts in the field of natural health and are manufactured according to the highest pharmaceutical standards for maximum safety and effectiveness. For more information, visit us at www.nativeremedies.com

Distributed by

Native Remedies, LLC

6531 Park of Commerce Blvd.

Suite 160

Boca Raton, FL 33487

Phone: 1.877.289.1235

International: + 1.561.999.8857

The letters HPUS indicate that the component(s) in this product is (are) officially monographed in the Homeopathic Pharmacopoeia of the United States.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

bottle labelbottle label

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep this and all medications out of reach of children.

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
68647-177-102019-10-21C16284748780-1956f9ecf-ccde-621f-e053-dbdaa90a74adSCAB-EASE ITCH RELIEF

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68647-177-10Scab Ease Itch Relief50000 mL in 1 BOTTLE, GLASSTINCTURE500003

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68647-177SCAB EASE ITCH RELIEF (PSORINUM , STAPHISAGRIA , VIOLA TRI ) TINCTURE [FEELGOOD HEALTH]3Legacy NDC, 1 package rows20100825_8fb9e0c6-8a0b-4fb0-9a78-e98201c38251.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
DELPHINIUM STAPHISAGRIA SEEDACTIVE INGREDIENT00543AP1JV3
SCABIES LESION LYSATE (HUMAN)ACTIVE INGREDIENT5UAU16Z1U43
VIOLA TRICOLORACTIVE INGREDIENT9Q24RAI43V3
DELPHINIUM STAPHISAGRIA SEEDACTIVE MOIETY00543AP1JV3
SCABIES LESION LYSATE (HUMAN)ACTIVE MOIETY5UAU16Z1U43
VIOLA TRICOLORACTIVE MOIETY9Q24RAI43V3
CITRUS PARADISI SEEDINACTIVE INGREDIENT12F08874Y73
WATERINACTIVE INGREDIENT059QF0KO0R3

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
68647-17768647-177-10

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
SCABIES LESION LYSATE (HUMAN)5UAU16Z1U4ACTIB
DELPHINIUM STAPHISAGRIA SEED00543AP1JVACTIB
VIOLA TRICOLOR9Q24RAI43VACTIB
CITRUS PARADISI SEED12F08874Y7IACT
WATER059QF0KO0RIACT

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
24c97740-6018-41fe-b1b9-5e2c949dbfe78fb9e0c6-8a0b-4fb0-9a78-e98201c382512010-07-28WarningsExact identifier
spl id: 24c97740-6018-41fe-b1b9-5e2c949dbfe7
spl set id: 8fb9e0c6-8a0b-4fb0-9a78-e98201c38251

Reported adverse events (FAERS/openFDA)#

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