Ellocy Wart remover

Manufacturer
Aramode
Effective date
2024-09-02
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:18:35

Label at a glance#

ProductEllocy Wart remover
Active ingredientSALICYLIC ACID
Label structure14 sections

Dosage and administration

• wash the affected area. • dry thoroughly • apply 2 times a day (2-3 applications each time). • continue application for 5-7 days.

Storage and handling

Store between 20 to 25℃ (68 to 77F) Protect from excessive heat above 40℃ (104F)

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Salicylic acid 1%

Purpose

OTC - PURPOSE SECTION

remove wart

Use

INDICATIONS & USAGE SECTION

• for removal of common and plantar warts
• the plantar wart is recognized by its location only on the bottom of the foot, its tenderness, and the interruption of the footprint pattern

Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

• On damaged skin (cuts, abrasions, eczema, sunburn).
• If you are pregnant or breastfeeding

When Using

OTC - WHEN USING SECTION

• Aviod contact with eyes.If product gets into the eyes, flush with water for 15 minutes.• If irritation persists, seek medical attention immediately.

Stop Use

OTC - STOP USE SECTION

if irritation occurs
if an allergic reaction occurs

Ask Doctor

OTC - ASK DOCTOR SECTION

if you are pregnant or breastfeeding
if you have diabetes

Keep Oot Of Reach Of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep Out Of Reach Of Children

Directions

DOSAGE & ADMINISTRATION SECTION

• wash the affected area.
• dry thoroughly
• apply 2 times a day (2-3 applications each time).
• continue application for 5-7 days.

Other information

STORAGE AND HANDLING SECTION

Store between 20 to 25℃ (68 to 77F)
Protect from excessive heat above 40℃ (104F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Fritillaria extract, Purslane extract, Safflower, Willow bark extract, Lactic acid, Borneol, Dimethyl sulfoxide, Chlorhexidine acetate

Questions

OTC - QUESTIONS SECTION

CUSTOMER SUPPORT Contact us at support@ellocy.com

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1047362salicylic acid 1 % Topical SolutionPSN1
1047362salicylic acid 10 MG/ML Topical SolutionSCD1
1047362salicylic acid 1 % Topical SolutionSY1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
f52be47f-7aa7-46c0-b1fa-50c18dd50206Product name120201029
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
dea2eded-d1e7-46bb-9a3d-f8dc20de6277Product name120190408
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
597b1cfd-7b31-5048-62be-ca5cd740da2fProduct name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
83596-004-012025-07-29C16284748780-13b156c62-31a5-fb37-e063-e6dba90a4e0783596-004

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83596-004-01Ellocy Wart remover5 mL in 1 BOTTLELIQUID51

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83596-004ELLOCY WART REMOVER (WART REMOVER) LIQUID [ARAMODE]11 package rows20240903_2120cbde-7dff-46a6-e063-6394a90a8e1a.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83596-00483596-004-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

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
2120cbde-7e00-46a6-e063-6394a90a8e1a2120cbde-7dff-46a6-e063-6394a90a8e1a2024-09-02WarningsExact identifier
spl id: 2120cbde-7e00-46a6-e063-6394a90a8e1a
spl set id: 2120cbde-7dff-46a6-e063-6394a90a8e1a

Reported adverse events (FAERS/openFDA)#

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