DR. SCHOLLS ULTRA THIN CORN REMOVERS salicylic acid disc

Country: United States

Language: English

Source: NLM (National Library of Medicine)

Active ingredient:

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

Available from:

Bayer Health Care LLC.

INN (International Name):

SALICYLIC ACID

Composition:

SALICYLIC ACID 0.4 g

Prescription type:

OTC DRUG

Authorization status:

OTC monograph final

Summary of Product characteristics

DR. SCHOLLS ULTRA THIN CORN REMOVERS- SALICYLIC ACID DISC
BAYER HEALTH CARE 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._
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DR. SCHOLL'S ULTRA THIN CORN REMOVERS
_DRUG FACTS_
ACTIVE INGREDIENT
Salicylic acid 40%
PURPOS E
Corn remover
US ES
for 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
wash affected area and dry thoroughly
if necessary, cut medicated disk to fit corn
apply medicated disk with sticky side adhering to skin
cover medicated disk with enclosed cover
after 48 hours , remove medicated disk
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 20° to 25°C (68° to 77°F)
Protect from excessive heat (temperatures above 40°C (104°F)).
INACTIVE INGREDIENTS
antioxidant (CAS 991-84-4), iron oxides, mineral oil, petroleum
hydrocarbon resin, silicon dioxide,
synthetic polyisoprene rubber, talc
QUES TIONS ?
866-360-3226
PRINCIPAL DISPLAY PANEL - 9 COVER/9 MEDICATED DISK CELLO PACK
DR. SCHOLLS ULTRA THIN CORN REMOVERS
salicylic acid disc
PRODUCT INFORMATION
PRODUCT T YPE
HUMAN OTC DRUG
ITE M CODE (SOURCE )
NDC:11523-0 6 29
ROUTE OF ADMINISTRATION
TOPICAL
Bayer Health Care LLC.
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRE NG TH
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)
SALICYLIC ACID
0 .4 g
INACTIVE INGREDIENTS
INGREDIENT NAME
STRE NG TH
MINERAL O IL (UNII: T5L8 T28 FGP)
SILICO N DIO XIDE (UNII: ETJ7Z6 XBU4)
TALC (UNII: 7SEV7J4R1U)
PRODUCT