Scholls Wellness Company LLC by Scapa Tapes North America LLC Corn Removers (Scapa)

Scholls Wellness Company LLC by

Drug Labeling and Warnings

Scholls Wellness Company LLC by is a Otc medication manufactured, distributed, or labeled by Scapa Tapes North America LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SCHOLLS WELLNESS COMPANY LLC CORN REMOVERS- salicylic acid disc 
Scapa Tapes North America LLC

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

----------

Corn Removers (Scapa)

Drug Facts

Drug Facts

Active Ingredient Purpose

Salicylic Acid 40%.......................Corn remover

Purpose

Corn remover

Uses

Uses

for the removal of corns
relieves pain by removing corns

Warnings

For external use only

Do not use

if you are a diabetic
if you have poor blood circulation
on irritated skin or any area that is infected or reddened

Stop use and ask a doctor if discomfort lasts

Keep out of reach of children. If swallowed,

get medical help or contact a Poison Control Center right away.

Directions

DURAGEL CORN CALLUS REMOVER

Directions​

wash affected area and dry thoroughly

if necessary, cut medicated disc to fit corn

apply medicated disc with sticky side adhering to skin

cover medicated disc with enclosed cushion

after 48 hours, remove medicated disc

repeat procedure every 48 hours as needed for up to 14 days (until corn is removed)

may soak callus in warm water for 5 minutes to assist in removal

Other Information

Other information​

store between 20ºC to 25ºC (68º to 77ºF).

Inactive ingredients​ antioxidant
(CAS 991-84-4), iron oxides, mineral oil,

petroleum hydrocarbon resin, silicon dioxide,

synthetic polyisoprene rubber, talc

Questions? 1-866-360-3226

SCHOLLS WELLNESS COMPANY LLC  CORN REMOVERS
salicylic acid disc

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 66843-067
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	0.4 g  in 1 g

Inactive Ingredients
Ingredient Name	Strength
MINERAL OIL (UNII: T5L8T28FGP)
TALC (UNII: 7SEV7J4R1U)
BROWN IRON OXIDE (UNII: 1N032N7MFO)

Product Characteristics
Color	brown	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 66843-067-81	9 in 1 CARTON	01/01/2021
1		1 g in 1 POUCH; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part358F	01/01/2021

Labeler - Scapa Tapes North America LLC (079995435)

Registrant - Scapa Tapes North America LLC (079995435)

Revised: 1/2022

Document Id: d673370e-42fa-dab0-e053-2a95a90a613a

34390-5

Set id: d6735398-70b1-7ccd-e053-2a95a90a0dfa

Version: 1

Effective Time: 20220125