SANI-PROFESSIONAL SANI-HANDS MADE WITH TENCEL- sani-hands 1ct swab

Country: United States

Language: English

Source: NLM (National Library of Medicine)

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Active ingredient:

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

Available from:

Professional Disposables International Inc.

Administration route:

TOPICAL

Prescription type:

OTC DRUG

Therapeutic indications:

Antimicrobial Hand sanitizer to decrease bacteria on the skin. Dries in seconds.

Authorization status:

OTC monograph not final

Summary of Product characteristics

                                SANI-PROFESSIONAL SANI-HANDS MADE WITH TENCEL- SANI-HANDS 1CT SWAB
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._
----------
NDC 10819-3922-1 SANI PROFESSIONAL SANI HANDS INDIVIDUAL PACKETS
ACTIVE INGREDIENT
65.9% alcohol by volume
PURPOSE
Antimicrobial
USES
Hand sanitizer to decrease bacteria on the skin. Dries in seconds.
WARNINGS
FLAMMABLE, KEEP AWAY FROM FIRE OR FLAME. FOR EXTERNAL USE ONLY. Do not
use in
or contact the eyes. Discontinue use if irritation and redness
develop. If condition
persists for more than 72 hours, consult a physician.
KEEP THIS OUT OF REACH OF CHILDREN
If swallowed, get medical help or contact a Poison Control Centerright
away
DIRECTIONS
Open packet. USe entire wpe to thoroughly wipe hands, fingers and
wrists.To sanitize,
useuse multiple wipes. Discard after single use.
INACTIVE INGREDIENTS
Water, Propylene Glycol, Glycerin, Aloe Barbedensis Leaf juice,
Tocopheryl Acetate
PRINCIPAL DISPLAY PANEL - 1 CT
Sani Professional Brand
Sani-Hands
Hand Instant Sanitizing Wipes
Kills 99.99% of germs
Cleans more effectively than gels
FDA Food Code Compliant
1 wipes individually wrapped
6.0 x 5.0 in (15.2 x 12.7 cm)
Packet:
SANI-PROFESSIONAL SANI-HANDS MADE WITH TENCEL
sani-hands 1ct swab
PRODUCT INFORMATION
PRODUCT TYPE
HUMAN OTC DRUG
ITEM CODE (SOURCE)
NDC:10819-3922
ROUTE OF ADMINISTRATION
TOPICAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRENGTH
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)
ALCOHOL
0.659 mL in 1 mL
INACTIVE INGREDIENTS
INGREDIENT NAME
STRENGTH
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
GLYCERIN (UNII: PDC6A3C0OX)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
WATER (UNII: 059QF0KO0R)
Professional Disposables International Inc.
PACKAGING
#
ITEM CODE
PACKAGE DESCRIPTION
MARKETING START
DATE
MARKETING END
DATE
1
NDC:10819
                                
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