Salicylic Acid (Medicated Callus Removers Extra Thick) Patch [Chain Drug Consortium, Llc] -

SALICYLIC ACID (MEDICATED CALLUS REMOVERS EXTRA THICK) PATCH [CHAIN DRUG CONSORTIUM, LLC]
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Active ingredient

Salicylic acid 40%
Purpose

Callus remover
Use
- for the removal of calluses
- relieves pain by removing calluses
Warnings
For external use only.
Do not use
- if you are a diabetic
- if you have poor blood circulation
- on irritated skin, on any area that is infected or reddened
Stop use and ask a doctor

if discomfort persists

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 area 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 corn is removed)
- may soak corn 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
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Premier Value

Extra Thick
CALLUS REMOVERS

Salicylic acid
- Callus removal treatment
- Relieves against pressure & pain
4 MEDICATED PATCHES/4 PADS

INGREDIENTS AND APPEARANCE

SALICYLIC ACID
medicated callus removers extra thick patch

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	40 mg in 4

Ingredient Name	Strength
Inactive Ingredients
POLYVINYL ALCOHOL (UNII: 532B59J990)
VINYL ACETATE (UNII: L9MK238N77)
HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:68016-230-04	4 in 1 PACKAGE; Type 0: Not a Combination Product	02/12/2018

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part358F	02/12/2018

Labeler - Chain Drug Consortium, LLC (101668460)

Registrant - Premier Brands of America (063849780)

Name	Address	ID/FEI	Business Operations
Establishment
Premier Brands of America		080051232	relabel(68016-230) , repack(68016-230)

Name	Address	ID/FEI	Business Operations
Establishment
Alchemix Corporation		615263956	manufacture(68016-230)

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Medic