SINSINPAS CORN REMOVER- salicylic acid patch

Country: United States

Language: English

Source: NLM (National Library of Medicine)

Active ingredient:

Salicylic Acid 40% ------------------------------ Corn, Callus and Wart Remover

Available from:

Sinsin Pharmaceutical Co., Ltd.

Administration route:

TOPICAL

Prescription type:

OTC DRUG

Therapeutic indications:

Corn, Callus and Wart Remover - for the removal of corns, calluses, warts

Authorization status:

OTC monograph final

Summary of Product characteristics

SINSINPAS CORN REMOVER- SALICYLIC ACID PATCH
SINSIN PHARMACEUTICAL CO., LTD.
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SINSINPAS CORN REMOVER PATCH
ACTIVE INGREDIENTS
Salicylic Acid 40% ------------------------------ Corn, Callus and
Wart Remover
PURPOSE
Corn, Callus and Wart Remover
USES
- for the removal of corns, calluses, warts
WARNINGS
WARNINGS
- For external use only
DO NOT USE
- if you are a diabetic or poor blood circulation
- on irritated skin or any area that is infected or reddened
- on the face, genital, or mucous membranes, on moles, birthmarks,
corns, warts with
hair growing from them
STOP USE AND ASK A DOCTOR IF discomfort persists
KEEP OUT OF REACH OF CHILDREN
KEEP OUT OF REACH OF CHILDREN.
If swallowed, get medical help or contact a Poison Control Center
(1-800-222-1222)
right away.
DIRECTIONS
- wash affected area and dry thoroughly
- apply medicated bandage
- after 48 hours, remove medicated bandage
- repeat procedure every 48 hours for up to 14 days for corn/callus
removal and up to
12 weeks for warts, until the problem has cleared.
- may soak corn in warm water for 5 minutes to assist in removal
OTHER INFORMATION
- store between 20℃ to 25℃ (68℉ to 77℉)
- protect from excessive heat and temperatures above 40℃ (104℉)
INACTIVE INGREDIENTS
Adhesive bandage, Felt, Glyceryl rosinate, Natural rubber, Non-woven
fabric,
Polyisobutylene, Purified lanolin, Releasing paper, Water-based
acrylic adhesive(BS-100)
PACKAGE LABEL
SINSINPAS CORN REMOVER
Sinsin Pharmaceutical Co., Ltd.
salicylic acid patch
PRODUCT INFORMATION
PRODUCT TYPE
HUMAN OTC DRUG
ITEM CODE (SOURCE)
NDC:55264-115
ROUTE OF ADMINISTRATION
TOPICAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRENGTH
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)
SALICYLIC ACID
25.6 mg in 100
INACTIVE INGREDIENTS
INGREDIENT NAME
STRENGTH
GLYCERYL ROSINATE (UNII: SD112V492J)
NATURAL LATEX RUBBER (UNII: 2LQ0UUW8IN)
LANOLIN (UNII: 7EV65EAW6H)
POLYISOBUTYLENE (1000 MW) (UNII: 5XB3A63Y52)
PACKAGING
#
ITEM CODE
PACKAGE DESCRIPTION
MARKETING S