FDA.reportPublic FDA data

WHP Be gone Skin Irritation

Manufacturer
Washington Homeopathic Products
Effective date
2014-05-08
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:08:48

Label at a glance#

ProductWHP Be gone Skin Irritation TM
Active ingredientARSENIC TRIOXIDE, CALCIUM SULFATE ANHYDROUS, SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE, SILICON DIOXIDE
Label structure8 sections

Indications and uses

Relieves symptoms associated with dry scaly skin with itching and burning usually occurring on the face, neck and insides of the knees and elbows.

Dosage and administration

Adults: 2 pills every 3 hours for 2 days. Then 2 pills morning and night for 2 weeks. Children: 1 pill. Repeat as necessary.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

ARSENICUM ALB

CALC SULPH

NAT PHOS

SILICEA

USES

OTC - PURPOSE SECTION

Relieves symptoms associated with dry scaly skin with itching and burning usually occurring on the face, neck and insides of the knees and elbows.

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

Indications:

ARSENICUM ALB   Scaley, red, dry

CALC SULPH   Slow healing

NAT PHOS   Smooth, red, shining

SILICEA   Boils, waxy, painful scars

STOP USE AND ASK DOCTOR

WARNINGS SECTION

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

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

Adults: 2 pills every 3 hours for 2 days. Then 2 pills morning and night for 2 weeks.

Children: 1 pill.

Repeat as necessary.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Sucrose/Lactose

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image of boximage of box

image of labelimage of label

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
bee4fa8d-8d82-423a-a0b5-40a89dd13a99Product name120250618
e0d2eb29-08bd-4bba-90d1-c91c68a38767Product name420250516
efd58dcf-540a-4531-8766-e713129ca6f2Product name120250307
30b0ac6e-02aa-0e5c-0d8b-cffdf3a282b2Product name520250304
4b7700e3-6e0e-45e5-9d22-6f754d61386eProduct name220250304
726062af-1135-4707-a1d7-57256991bbf9Product name220250226
63f39a63-5cd1-4016-bd86-2bbb0f6c3139Product name320240506
e5a77e9c-c528-733a-173d-914a234c024bProduct name520240506
334fe8d2-68fb-4331-a576-420e302ec069Product name720240320
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
e92765c1-be81-432a-b909-1b10777ec378Product name120190208
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
0441a8f5-3835-497c-aedd-bc78cba56b2aProduct name120150317
19c71a3d-ed9c-166b-a7e5-38c250c35631Product name120140508
87711080-88eb-65c5-b2dd-bf99e700a372Product name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
68428-749-292025-01-30C16284748780-12cef2736-71bf-d83d-e063-dadaa90ab31fDRUG FACTS

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68428-749-14WHP Be gone Skin IrritationTM300 in 1 BOTTLE, PLASTICPELLET3001
68428-749-29WHP Be gone Skin IrritationTM1 in 1 BOXPELLET11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68428-749WHP BE GONE SKIN IRRITATION TM (ARSENIC TRIOXIDE - CALCIUM SULFATE ANHYDROUS - SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE - SILICON DIOXIDE) PELLET [WASHINGTON HOMEOPATHIC PRODUCTS]1Legacy NDC, 2 package rows20170609_46b2e90f-b9b4-4352-a184-6a870aaf91f5.zip

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
68428-74968428-749-14, 68428-749-29

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
ARSENIC TRIOXIDES7V92P67HOACTIB
SUCROSEC151H8M554IACT
LACTOSEJ2B2A4N98GIACT
CALCIUM SULFATE ANHYDROUSE934B3V59HACTIB
SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE70WT22SF4BACTIB
SILICON DIOXIDEETJ7Z6XBU4ACTIB

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
3323800d-6584-41fa-95e2-0a0aadcee36246b2e90f-b9b4-4352-a184-6a870aaf91f52014-05-08WarningsExact identifier
spl id: 3323800d-6584-41fa-95e2-0a0aadcee362
spl set id: 46b2e90f-b9b4-4352-a184-6a870aaf91f5

Reported adverse events (FAERS/openFDA)#

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