FREDS MEDICATED ANTI ITCH- pramoxine hydrochloride, menthol cream

Χώρα: Ηνωμένες Πολιτείες

Γλώσσα: Αγγλικά

Πηγή: NLM (National Library of Medicine)

Δραστική ουσία:

PRAMOXINE HYDROCHLORIDE (UNII: 88AYB867L5) (PRAMOXINE - UNII:068X84E056), MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)

Διαθέσιμο από:

Discount Drug Mart

Οδός χορήγησης:

TOPICAL

Τρόπος διάθεσης:

OTC DRUG

Θεραπευτικές ενδείξεις:

for the temporary relief of pain and itching due to: minor burns, sunburn, minor cuts, scrapes, insect bites, minor skin irritations ,minor rashes due to poison ivy, poison oak, or poison sumac Topical anagesic

Καθεστώς αδειοδότησης:

OTC monograph not final

Αρχείο Π.Χ.Π.

FREDS MEDICATED ANTI ITCH- PRAMOXINE HYDROCHLORIDE, MENTHOL CREAM
DISCOUNT DRUG MART
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DISCOUNT DRUG MART MEDICATED ANTI ITCH CREAM
ACTIVE INGREDIENT
Menthol 1%
Pramoxine hydrochloride 1%
USES
for the temporary relief of pain and itching due to: minor burns,
sunburn, minor cuts,
scrapes, insect bites, minor skin irritations ,minor rashes due to
poison ivy, poison oak,
or poison sumac
PURPOSE
Topical anagesic
WARNINGS
WHEN USING THIS PRODUCT
do not get into eyes
KEEP OUT OF REACH OF CHILDREN
If swallowed, get medical help or contact a Poison Control Center
right away.
OTHER INFORMATION
store at controlled room temperature
DIRECTIONS
adults and children 2 years and older: apply to affected area not more
than 3 to 4 times
daily
children under 2 years: consult a doctor
Adults and Children 2 years and older: Apply to affected are not more
than 3 to 4 times
daily.
INACTIVE INGREDIENTS
aloe barbadensis (aloe vera) leaf juice, diazolidinyl urea, edetate
disodium, eucalyptus oil,
aloe barbadensis (aloe vera) leaf juice, diazolidinyl urea, edetate
disodium, eucalyptus oil,
methylparaben, methyl salicylate, mineral oil, PPG-1 trideceth-6,
propylene glycol,
propylparaben, purified water, sodium acrylates copolymer,
steareth-21, stearyl alcohol,
tocopheryl acetate, trolamine, white petrolatum
FREDS MEDICATED ANTI ITCH
pramoxine hydrochloride, menthol cream
PRODUCT INFORMATION
PRODUCT TYPE
HUMAN OTC DRUG
ITEM CODE (SOURCE)
NDC:53943-265
ROUTE OF ADMINISTRATION
TOPICAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRENGTH
PRAMOXINE HYDROCHLORIDE (UNII: 88AYB867L5) (PRAMOXINE -
UNII:068X84E056)
PRAMOXINE
HYDROCHLORIDE
1 g
in 100 g
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)
MENTHOL
1 g
in 100 g
INACTIVE INGREDIENTS
INGREDIENT NAME
STRENGTH
STEARETH-21 (UNII: 53J3F32P58)
.ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)
SODIUM ACRYLATE (UNII: 7C98FKB43H)
MINERAL OIL (UNII: T5L8T28FGP)
EDETATE DISODIUM (UNII: 7FLD91C86K)
TROLAMINE (UNII: 9O3K93S3TK)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
METH