FDA.reportPublic FDA data

VERUCIDE WART REMOVER Kit

Manufacturer
Blaine Labs Inc.
Effective date
2025-01-02
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 00:50:30

Label at a glance#

ProductVERUCIDE WART REMOVER Kit
Active ingredientALCOHOL, SALICYLIC ACID
Label structure10 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Drug Facts

Active Ingredient(in step 1)...................... Alcohol 60%

Active Ingredient(in step 2)  ............. Salicylic Acid 17%

OTC - PURPOSE SECTION

Purpose

Alcohol 60% (step 1) ............................................................... Antiseptic

Salicylic Acid 17% (step 2) ................................................ Wart Remover

INDICATIONS & USAGE SECTION

Uses
■ (for step 1)Antiseptic to decrease bacteria on the skin
■ (for step 2)For the removal of common warts. The common wart is
easily recognized by the rough “cauliflower-like” appearance of the
surface ■ For the removal of plantar warts on the bottom of the foot. 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 SECTION

Warnings- For external use only (for step 1 & 2)
Extremely flammable. Keep away from fire or flames

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.Stop use and consult a doctor if discomfort
persists. Avoid contact with the eyes. If contact with eye occurs, wash
thoroughly with water

OTC - WHEN USING SECTION

When using step 2, do not use: on irritated skin, any area that is infected or
reddened, if you are diabetic, have poor blood circulation, moles, birthmarks,
genital warts, warts with hair growing from them, warts on the face, or
mucous membranes

If swallowed, get medical help or contact a poison control center
right away 1-800-222-1222

DOSAGE & ADMINISTRATION SECTION

Directions

■ (for step 1)Wash the affected area
with one or two drops
■ ( for step 2)Clean using step 1 and
allow area to dry. Apply a small
amount at a time with applicator to
sufficiently cover each wart and let
dry ■ Let dry ■ Repeat this procedure
once or twice daily as needed (until
wart is removed) for up to 12 weeks

OTHER SAFETY INFORMATION

Other Information

Store at room temperature: 20-27ºC
(68-81ºF)

INACTIVE INGREDIENT SECTION

Inactive Ingredients

(for step 1)
Glycerin, Hydroxypropyl Cellulose,
Lavandula Angustifolia (Lavender)
Flower Extract, Purified Water

(for step 2)
Alcohol (Ethanol), Artemisia
Absinthium (Wormwood) Extract,
Carica Papaya (Papaya) Fruit Extract,
Glycerin, Hydroxypropyl Cellulose,
Purified Water

OTC - QUESTIONS SECTION

Questions or Comments?
800.307.8818 | BlaineLabs.com
M-F, 7:30 AM - 4:00 PM (pst)
Contact@BlaineLabs.com

VERUCIDE ®Wart Remover Kit Labeling

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BLAINE LABS `               NDC 63347-720-01

VERUCIDE ®
WART REMOVER

TWO-STEP WART TREATMENT KIT

SALICYLIC ACID
IN A SOLUTION CONTAINING
ALCOHOL AND PAPAYA EXTRACT

KIT INCLUDES:
STEP 1: 0.253 FL OZ (7.5 mL)
STEP 2: 0.101 FL OZ (3.0 mL)

Manufactured By:
Blaine Labs, Inc.
11037 Lockport Place
Santa Fe Springs, CA 90670

Verucide 750 KitVerucide 750 Kit

Step1

721 Step1721 Step1

Step2

722 Step2722 Step2

res

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1039483ethanol 60 % Topical SolutionPSN3
312881salicylic acid 17 % Topical SolutionPSN3
1039483ethanol 0.6 ML/ML Topical SolutionSCD3
312881salicylic acid 170 MG/ML Topical SolutionSCD3
1039483ethanol 60 % Topical SolutionSY3
312881salicylic acid 17 % Topical SolutionSY3

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
3c386306-c48a-413e-bb69-70cb268496f3Product name120210727
dea2eded-d1e7-46bb-9a3d-f8dc20de6277Product name120190408
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
63347-720-01VERUCIDE WART REMOVER Kit1 in 1 PACKAGEKIT13
63347-721-01VERUCIDE WART REMOVER Kit7.5 mL in 1 BOTTLELIQUID7.5 mL60 g in 100mL3
63347-722-01VERUCIDE WART REMOVER Kit3 mL in 1 BOTTLELIQUID3 mL17 g in 100mL3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
63347-720VERUCIDE WART REMOVER KIT (WART REMOVER) KIT [BLAINE LABS INC.]3Current NDC, 3 package rows20250104_017f3ca2-6dba-4db5-b559-8ce0f2709772.zip
63347-721VERUCIDE WART REMOVER KIT (WART REMOVER) KIT [BLAINE LABS INC.]3Unmatched20250104_017f3ca2-6dba-4db5-b559-8ce0f2709772.zip
63347-722VERUCIDE WART REMOVER KIT (WART REMOVER) KIT [BLAINE LABS INC.]3Unmatched20250104_017f3ca2-6dba-4db5-b559-8ce0f2709772.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
63347-72063347-720-01
63347-72163347-721-01
63347-72263347-722-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
NameUNIIKind
GLYCERINPDC6A3C0OXIACT
HYDROXYPROPYL CELLULOSE, UNSPECIFIED9XZ8H6N6OHIACT
LAVANDULA ANGUSTIFOLIA SUBSP. ANGUSTIFOLIA FLOWER19AH1RAF4MIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
ALCOHOL3K9958V90MIACT
WORMWOODF84709P2XVIACT
PAPAYAKU94FIY6JBIACT
GLYCERINPDC6A3C0OXIACT
HYDROXYPROPYL CELLULOSE, UNSPECIFIED9XZ8H6N6OHIACT
WATER059QF0KO0RIACT
SALICYLIC ACIDO414PZ4LPZACTIB

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
VERUCIDE WART REMOVER KitWART REMOVERBlaine Labs Inc.017f3ca2-6dba-4db5-b559-8ce0f27097722025-01-02WarningsExact identifier
ndc (package): 63347-722-01
ndc (package): 63347-721-01
ndc (package): 63347-720-01
ndc (product): 63347-720
ndc11 (package): 63347072001
ndc11 (package): 63347072101
ndc11 (package): 63347072201
spl id: 8d1b445c-d868-4bc9-855a-785d3b33112e
spl set id: 017f3ca2-6dba-4db5-b559-8ce0f2709772

Reported adverse events (FAERS/openFDA)#

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