SALICYLIC ACID CORN REMOVER- salicylic acid strip

Salicylic Acid Corn Remover by

Drug Labeling and Warnings

Salicylic Acid Corn Remover by is a Otc medication manufactured, distributed, or labeled by ASO Pharmaceutical Co. Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Salicylic acid 40%

Purpose

Corn remover

Uses

• for the removal of corns.
• relieves pain by removing corns

Warnings

For External Use Only

Do not use

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

Stop use and ask a doctor if

discomfort lasts

Keep out of reach of children.

In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

Directions

• Wash affected area and dry thoroughly
• Remove medicated pad from backing paper by pulling from center of pad
• Apply
• After 48 hours, remove medicated pad
• Repeat procedure every 48 hours as needed for up to 14 days (until corn is removed)
• May soak corn in warm water for 5 minutes to assist in removal

Other information

• store at room temperature
• avoid excessive heat 99ºF (37ºC)

Inactive ingredients

lanolin, polybutene, rosin ester, rubber

SPL UNCLASSIFIED SECTION

Distributed by:

ASO LLC
Sarasota, FL 34240

Made in Japan

*This product is not manufactured or distributed by he Bayer Corporation, owners of the registered trademark Dr. Scholl’s®.

Principal Display Panel

Compare to the active ingredient in Dr. Scholl’s®*

ONE STEP

CORN REMOVER

MAXIMUM STRENGTH

SALICYLIC ACID 40%

• Cushions & helps relieve pain
• Convenient 1-step bandage
• Waterproof

6 MEDICATED BANDAGES

INGREDIENTS AND APPEARANCE

SALICYLIC ACID CORN REMOVER 
salicylic acid strip

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 51511-514
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	40 mg

Inactive Ingredients
Ingredient Name	Strength
LANOLIN (UNII: 7EV65EAW6H)
NATURAL LATEX RUBBER (UNII: 2LQ0UUW8IN)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 51511-514-01	1 in 1 BOX	02/01/2010
1		6 in 1 POUCH; Type 0: Not a Combination Product
2	NDC: 51511-514-24	2400 in 1 CARTON	02/01/2010
2		200 in 1 TRAY
2		6 in 1 POUCH; Type 0: Not a Combination Product
3	NDC: 51511-514-18	1800 in 1 CARTON	01/08/2010
3		150 in 1 TRAY
3		8 in 1 POUCH; Type 0: Not a Combination Product
4	NDC: 51511-514-08	1 in 1 BOX	01/08/2010
4		8 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	part358B	01/08/2010

Labeler - ASO Pharmaceutical Co. Ltd. (690629019)