Dr Scholl's ® One Step Corn REMOVERS

País: Estados Unidos

Língua: inglês

Origem: NLM (National Library of Medicine)

Ingredientes ativos:

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

Disponível em:

Bayer HealthCare LLC.

DCI (Denominação Comum Internacional):

SALICYLIC ACID

Composição:

SALICYLIC ACID 0.4 g

Via de administração:

TOPICAL

Tipo de prescrição:

OTC DRUG

Indicações terapêuticas:

Corn remover - for removal of corns - relieves pain by removing corns

Status de autorização:

OTC monograph final

Características técnicas

DR. SCHOLLS ONE STEP CORN REMOVERS- SALICYLIC ACID DISC
BAYER HEALTHCARE 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._
----------
DR SCHOLL'S
ONE
STEP
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
apply medicated bandage
after 48 hours , remove medicated bandage
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 - 6 STRIP CARTON
DR. SCHOLLS ONE STEP CORN REMOVERS
salicylic acid disc
Bayer HealthCare LLC.
PRODUCT INFORMATION
PRODUCT T YPE
HUMAN OTC DRUG
ITE M CODE (SOURCE )
NDC:11523-0 753
ROUTE OF ADMINISTRATION
TOPICAL
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 CHARACTERISTICS
COLOR
bro wn (o paque so lid)
S CORE
S HAP E
S IZ E
FLAVOR
IMPRINT CODE
CONTAINS
PACKAG ING
#
ITEM CODE
PACKAGE DESC