SALICYLIC ACID- medicated callus removers patch

Country: United States

Language: English

Source: NLM (National Library of Medicine)

Active ingredient:

SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)

Available from:

Chain Drug Consortium, LLC

INN (International Name):

SALICYLIC ACID

Composition:

SALICYLIC ACID 40 mg in 4

Administration route:

TOPICAL

Prescription type:

OTC DRUG

Therapeutic indications:

Callus remover - for the removal of calluses - relieves pain by removing calluses

Authorization status:

OTC monograph final

Summary of Product characteristics

SALICYLIC ACID- MEDICATED CALLUS REMOVERS PATCH
CHAIN DRUG CONSORTIUM, LLC
----------
PREMIER VALUE MEDICATED CALLUS REMOVERS
_​ACTIVE INGREDIENT_
Salicylic acid 40%
_PURPOSE_
Callus remover
_USES_
for the removal of calluses
relieves pain by removing calluses
_WARNINGS_
FOR EXTERNAL USE ONLY.
​DO NOT USE
if you are a diabetic
have poor blood circulation
on irritated skin, on any area that is infected or reddened
ASK YOUR DOCTOR
IF DISCOMFORT PERSISTS see your doctor or podiatrist.
KEEP OUT OF REACH OF CHILDREN.
If swallowed, get medical help or contact a Poison Control Center
right away.
_DIRECTIONS_
wash affected area and dry thoroughly
if necessary, cut medicated patch to fit callus
apply adhesive side down of medicated patch onto callus
cover medicated patch with pad
after 48 hours, remove medicated patch
repeat procedure every 48 hours as needed for up to 14 days (until
callus is
removed)
may soak callus in warm water for 5 minutes to assist in removal
_OTHER INFORMATION_
store between 15°C to 30°C (59°F to 86°F)
_INACTIVE INGREDIENTS_
acrylic adhesive, acrylic polymer, polyethylene, polyvinyl alcohol
_QUESTIONS?_
call 1-866-964-0939
PRINCIPAL DISPLAY PANEL
Premier Value
_MEDICATED_
_CALLUS_
_REMOVERS_
Salicylic Acid 40%
Effective callus removal treatment
Protects against pressure and friction
6 PADS
4 MEDICATED PATCHES
SALICYLIC ACID
medicated callus removers patch
PRODUCT INFORMATION
PRODUCT TYPE
HUMAN OTC DRUG
ITEM CODE (SOURCE)
NDC:68016-607
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 in 4
Chain Drug Consortium, LLC
INACTIVE INGREDIENTS
INGREDIENT NAME
STRENGTH
POLYVINYL ALCOHOL (UNII: 532B59J990)
VINYL ACETATE (UNII: L9MK238N77)
HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)
PACKAGING
#
ITEM CODE
PACKAGE DESCRIPTION
MARKETING START
DATE
MARKETING END
DATE
1
NDC:68016-607-
00
4 in 1 PACKAGE; Type 0: Not a Combination
Product
05/23/2003
MARKETING IN