PREMIUM HAND SANITIZER- ethanol gel

Χώρα: Ηνωμένες Πολιτείες

Γλώσσα: Αγγλικά

Πηγή: NLM (National Library of Medicine)

Δραστική ουσία:

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

Διαθέσιμο από:

MCKESSON MEDICAL-SURGICAL INC.

Οδός χορήγησης:

TOPICAL

Τρόπος διάθεσης:

OTC DRUG

Θεραπευτικές ενδείξεις:

Uses - an antiseptic hand sanitizer for topical application - helps prevent infection and cross-contamination - reduces transient microorganisms on intact skin - recommended for repeated use McKesson Premium Hand Sanitizer With Vitamin E, Moisturizers, & Emollients For frequent use

Καθεστώς αδειοδότησης:

OTC monograph not final

Αρχείο Π.Χ.Π.

PREMIUM HAND SANITIZER- ETHANOL GEL
MCKESSON MEDICAL-SURGICAL INC.
_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._
----------
_ACTIVE INGREDIENT PURPOSE_
Ethanol 70% ...................................... hand sanitizer
_USES_
an antiseptic hand sanitizer for topical application
helps prevent infection and cross-contamination
reduces transient microorganisms on intact skin
recommended for repeated use
KEEP OUT OF REACH OF CHILDREN. If swallowed, get medical help or
contact a Poison
Control Center right away.
McKesson Premium Hand Sanitizer
With Vitamin E, Moisturizers, & Emollients
For frequent use
_DIRECTIONS_
Wet hands thoroughly with product. Allow to dry without wiping. Use no
water or
towels.
_WARNINGS_
FOR EXTERNAL USE ONLY.
FLAMMABLE, KEEP AWAY FROM FIRE OR FLAME.
WHEN USING THIS PRODUCT
avoid contact with eyes. In case of eye contact, flush with
water for 15 minutes.
DISCONTINUE USE AND SEE A DOCTOR IF irritation occurs.
Avoid contact with broken skin.
_INACTIVE INGREDIENTS_
purified water, carbomer, glycerin, isopropyl myristate, tocopherol
(vitamin E),
diisopropyl sebacate, isopropanol, propylene glycol, aminomethyl
propanol, fragrance,
blue 1.
PREMIUM HAND SANITIZER
ethanol gel
PRODUCT INFORMATION
PRODUCT TYPE
HUMAN OTC DRUG
ITEM CODE (SOURCE)
NDC:68599-5201
ROUTE OF ADMINISTRATION
TOPICAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRENGTH
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)
ALCOHOL
70 g in 100 g
INACTIVE INGREDIENTS
INGREDIENT NAME
STRENGTH
WATER (UNII: 059QF0KO0R)
CARBOMER COPOLYMER TYPE A (UNII: 71DD5V995L)
GLYCERIN (UNII: PDC6A3C0OX)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
TOCOPHEROL (UNII: R0ZB2556P8)
DIISOPROPYL SEBACATE (UNII: J8T3X564IH)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
FD&C BLUE NO. 1 (UNII: