CAREALL TOLNAFTATE- tolnaftate cream

Valsts: Amerikas Savienotās Valstis

Valoda: angļu

Klimata pārmaiņas: NLM (National Library of Medicine)

Aktīvā sastāvdaļa:

Tolnaftate (UNII: 06KB629TKV) (Tolnaftate - UNII:06KB629TKV)

Pieejams no:

New World Imports, Inc

Ievadīšanas:

TOPICAL

Receptes veids:

OTC DRUG

Ārstēšanas norādes:

Antifungal - Proven clinically effective in the treatment of athlete's foot (tinea pedis), jock itch (tinea cruris), ringworm (tinea corporis) - For effective relief of itching, burning and cracking

Autorizācija statuss:

OTC monograph final

Produkta apraksts

CAREALL TOLNAFTATE- TOLNAFTATE CREAM
NEW WORLD IMPORTS, INC
----------
DRUG FACTS
Tolnaftate 1%
Antifungal
KEEP OUT OF REACH OF CHILDREN. If Swallowed, get medical help or
contact a Poison
Control center right away.
Proven clinically effective in the treatment of athlete's foot (tinea
pedis), jock itch
(tinea cruris), ringworm (tinea corporis)
For effective relief of itching, burning and cracking
FOR EXTERNAL USE ONLY
WHEN USING THIS PRODUCT avoid contact with the eyes
STOP USE AND ASK A DOCTOR IF
irritation occurs
there is no improvement within 4 weeks (for athlete's foot or ring
worm) or 2 weeks
(for jock itch).
DO NOT USE on children under 2 years of age unless directed by a
doctor
Wash affected area and dry thoroughly
Apply a thin layer over affected area twice daily (morning and night)
or as directed by
a doctor
Supervise children in the use of this product
for athlete's foot, pay special attention to spaces between the toes,
wear well-fitting,
ventilated shows and change shoes and socks at least once daily
For athlete's foot and ringworm use daily for 4 weeks, for jock itch
use daily for 2
weeks.
If condition persists longer consult a doctor
This product is not effective on scalp or nails
Ceteth 20, Cetyl Alcohol, Methylparaben, Mineral Oil, Propylene
Glycol, Propylparaben,
Sorbitan Monostearate, Steryl Alcohol, Purified Water
CAREALL TOLNAFTATE
tolnaftate cream
PRODUCT INFORMATION
PRODUCT TYPE
HUMAN OTC DRUG
ITEM CODE (SOURCE)
NDC:51824-001
ROUTE OF ADMINISTRATION
TOPICAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRENGTH
TOLNAFTATE (UNII: 06KB629TKV) (Tolnaftate - UNII:06KB629TKV)
Tolnaftate
10 mg in 1 g
INACTIVE INGREDIENTS
INGREDIENT NAME
STRENGTH
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
MINERAL OIL (UNII: T5L8T28FGP)
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
CETYL ALCOHOL (UNII: 936JST6JCN)
SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)
CETETH-20 (UNII: I835H2IHHX)
WATER (UNII: 059QF0KO0R)
METHYLPARABEN (UNII: A2I8C7HI9T)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
PRODUCT CHARACTERISTICS
COLOR
white
SCORE