PDI SANI-HANDS INSTANT HAND SANITIZING WIPES- alcohol cloth

Negara: Amerika Serikat

Bahasa: Inggris

Sumber: NLM (National Library of Medicine)

Beli Sekarang

Unduh Karakteristik produk (SPC)
20-10-2022

Bahan aktif:

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

Tersedia dari:

Professional Disposables International, Inc.

Rute administrasi :

TOPICAL

Jenis Resep:

OTC DRUG

Indikasi Terapi:

To decrease bacteria on the skin Antiseptic

Status otorisasi:

OTC monograph not final

Karakteristik produk

                                PDI SANI-HANDS INSTANT HAND SANITIZING WIPES- ALCOHOL CLOTH
PROFESSIONAL DISPOSABLES INTERNATIONAL, 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._
----------
PDI SANI HANDS
USES
To decrease bacteria on the skin
WARNINGS
FOR EXTERNAL USE ONLY
FLAMMABLE, KEEP AWAY FROM FIRE OR FLAME
WHEN USING THIS PRODUCT avoid contact with eyes. If contact occurs,
rinse eyes
thoroughly with water
DO NOT USE in or contact with eyes.
STOP USE AND ASK A DOCTOR if irritation and redness develop. If
condition persists
for more than 72 hours, consult a doctor.
INACTIVE INGREDIENTS
Aloe Barbadensis Leaf Juice, Glycerin, Propylene Glycol, Purified
Water, Tocopheryl
Acetate
ACTIVE INGREDIENT
Ethyl Alcohol 70% by volume
PURPOSE
Antiseptic
DIRECTIONS
Tear open packet
Open and unfold wipe
Thoroughly wipe hands, fingers and wrists using entire
Allow to dry
For dirty hands, use first wipe to clean hands, then discard wipe.
Sanitize with second
wipe.
Discard after single use
KEEP OUT OF REACH OF CHILDREN unless under adult supervision.
If swallowed, get medical help or contact a Poison Control Center
immediately.
OTHER INFORMATION
Lot No. and Expiration Date can be found on packet.
packet
box
PDI SANI-HANDS INSTANT HAND SANITIZING WIPES
alcohol cloth
Professional Disposables International, Inc.
PRODUCT INFORMATION
PRODUCT TYPE
HUMAN OTC DRUG
ITEM CODE (SOURCE)
NDC:10819-3916
ROUTE OF ADMINISTRATION
TOPICAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRENGTH
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)
ALCOHOL
0.7 mL in 1 mL
INACTIVE INGREDIENTS
INGREDIENT NAME
STRENGTH
WATER (UNII: 059QF0KO0R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
GLYCERIN (UNII: PDC6A3C0OX)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
PACKAGING
#
ITEM CODE
PACKAGE DESCRIPTION
MARKETING START
DATE
MARKETING END
DATE
1
NDC:10819-
3916-1
100 in 1 BOX
0
                                
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