VERUCIDE WART REMOVER KIT- wart remover kit

VERUCIDE WART REMOVER Kit by

Drug Labeling and Warnings

VERUCIDE WART REMOVER Kit by is a Otc medication manufactured, distributed, or labeled by Blaine Labs Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Drug Facts

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

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

PURPOSE

Purpose

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

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

INDICATIONS & USAGE

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

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

KEEP OUT OF REACH OF CHILDREN

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

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

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

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

QUESTIONS

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

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

Step1

Step2

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INGREDIENTS AND APPEARANCE

VERUCIDE WART REMOVER KIT 
wart remover kit

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 63347-720

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 63347-720-01	1 in 1 PACKAGE	09/29/2023

Quantity of Parts
Part #	Package Quantity	Total Product Quantity
Part 1	1 BOTTLE	7.5 mL
Part 2	1 BOTTLE	3 mL

Part 1 of 2

WART REMOVER STEP 1 
alcohol liquid

Product Information
Item Code (Source)	NDC: 63347-721
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	60 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
HYDROXYPROPYL CELLULOSE, UNSPECIFIED (UNII: 9XZ8H6N6OH)
LAVANDULA ANGUSTIFOLIA SUBSP. ANGUSTIFOLIA FLOWER (UNII: 19AH1RAF4M)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 63347-721-01	7.5 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	10/01/2023

Part 2 of 2

WART REMOVER STEP 2 
salicylic acid liquid

Product Information
Item Code (Source)	NDC: 63347-722
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	17 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ALCOHOL (UNII: 3K9958V90M)
WORMWOOD (UNII: F84709P2XV)
PAPAYA (UNII: KU94FIY6JB)
GLYCERIN (UNII: PDC6A3C0OX)
HYDROXYPROPYL CELLULOSE, UNSPECIFIED (UNII: 9XZ8H6N6OH)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 63347-722-01	3 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M028	10/01/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M028	09/29/2023

Labeler - Blaine Labs Inc. (017314571)

Registrant - Blaine Labs Inc. (017314571)