SANI MOUSSE- alcohol aerosol, foam

Χώρα: Ηνωμένες Πολιτείες

Γλώσσα: Αγγλικά

Πηγή: NLM (National Library of Medicine)

Αγόρασέ το τώρα

Αρχείο Π.Χ.Π. Αρχείο Π.Χ.Π. (SPC)
04-09-2012

Δραστική ουσία:

ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)

Διαθέσιμο από:

Superior Chemical Corporation

Οδός χορήγησης:

TOPICAL

Τρόπος διάθεσης:

OTC DRUG

Θεραπευτικές ενδείξεις:

Antiseptic for hand-washing to decrease bacteria on the skin, only when water is not available irritation and redness develop

Καθεστώς αδειοδότησης:

OTC monograph not final

Αρχείο Π.Χ.Π.

                                SANI MOUSSE - ALCOHOL AEROSOL, FOAM
SUPERIOR CHEMICAL CORPORATION
_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._
----------
SANI MOUSSE 4773 DRUG FACTS AND LABEL
DRUG FACTS BOX OTC-ACTIVE INGREDIENTS SECTION
Ethyl Alcohol 62%
DRUG FACTS BOX OTC-PURPOSE SECTION
Antiseptic
for hand-washing to decrease bacteria on the skin, only when water is
not available
DRUG FACTS BOX OTC-WARNINGS SECTION
Flammable, keep away from fire and flames
For external use only
DRUG FACTS BOX OTC-WHEN USING SECTION
do not get into eyes
if contact occurs, rinse eyes thoroughly with water
DRUG FACTS BOX OTC-STOP USE SECTION
irritation and redness develop
DRUG FACTS BOX OTC-KEEP OUT OF REACH OF CHILDREN SECTION
If swallowed, get medical help or contact a Poison Control Center
right away
DRUG FACTS BOX OTC-DOSAGE & ADMINISTRATION SECTION
Press valve once to deliver one squirt (about a quarter size) of
foaming product into the palm of your
hand
rub hands together and allow to dry without wiping
DRUG FACTS BOX OTC-INACTIVE INGREDIENTS SECTION
water, DEA-C8-18 perfluoroalkylethyl phosphate, cetearyl alcohol,
polysorbate 65, dimethicone PEG-
8 meadowfoamate, meadowfoamamidopropyl betaine, butane, propane,
fragrance
SANI MOUSSE 4773 199G
477307P4060.jpg
SANI MOUSSE
alcohol aerosol, foam
PRODUCT INFORMATION
PRODUCT T YPE
HUMAN OTC DRUG
ITE M CODE (SOURCE )
NDC:53125-773
ROUTE OF ADMINISTRATION
TOPICAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRE NG TH
ALCO HO L (UNII: 3K9 9 58 V9 0 M) (ALCOHOL - UNII:3K9 9 58 V9 0 M)
ALCOHOL
6 20 mg in 1 g
INACTIVE INGREDIENTS
INGREDIENT NAME
STRE NG TH
Superior Chemical Corporation
PRO PANE (UNII: T75W9 9 11L6 )
BUTANE (UNII: 6 LV4FOR43R)
WATER (UNII: 0 59 QF0 KO0 R)
PACKAG ING
#
ITEM CODE
PACKAGE DESCRIPTION
MARKETING START DATE
MARKETING END DATE
1
NDC:53125-773-25
19 9 g in 1 CAN
2
NDC:53125-773-26
454 g in 1 CAN
MARKETING INFOR
                                
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