BROOKSTONE ADVANCED HAND SANITIZER CLEAR FRESH- alcohol gel

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:

Argento sc by sicura inc.

Administration route:

TOPICAL

Prescription type:

OTC DRUG

Therapeutic indications:

Purpose:  Antimicrobial Decrease bacteria on skin that could cause disease Recommended for repeated use if irrigation and redness develop and condition persists for more than 72 hours

Authorization status:

OTC monograph not final

Summary of Product characteristics

                                BROOKSTONE ADVANCED HAND SANITIZER CLEAR FRESH- ALCOHOL GEL
ARGENTO SC BY SICURA 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(S)
Ethyl Alcohol 63% v/v
Purpose:
Antimicrobial
USE
Decrease bacteria on skin that could cause disease
Recommended for repeated use
WARNINGS
For external use only. Flammable, keep way from flame or fire
WHEN USING THIS PRODUCT
When using this product, keep out of eyes. In case of contact with
eyes, flush thoroughly with water
Do not ingest or inhale
Avoid contact with broken skin
STOP USE AND ASK A DOCTOR
if irrigation and redness develop and condition persists for more than
72 hours
KEEP OUT OF REACH OF CHILDREN
if swallowed,get medical help or contact a Poison Control Center
immediately
DIRECTIONS
Spread product on hands thoroughly and allow to dry, do not wipe off
For children under 6, use under adult supervision
Not recommended for use with infants
OTHER INFORMATION
Do not store above 105F (40.6C)
May discolor some fabrics
Harmful to plastics and wood finishes
INACTIVE INGREDIENTS
Purified water, Carbomer, Triethanolamine, Aloe Barbadensis Leaf
Juice, Vitamin E, Fragrance
BROOKSTONE ADVANCED HAND SANITIZER CLEAR FRESH
alcohol gel
PRODUCT INFORMATION
PRODUCT T YPE
HUMAN OTC DRUG
ITE M CODE (SOURCE )
NDC:77731-0 0 5
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 3 mL in 10 0 mL
INACTIVE INGREDIENTS
INGREDIENT NAME
STRE NG TH
CARBO MER 9 4 0 (UNII: 4Q9 3RCW27E)
TRO LAMINE (UNII: 9 O3K9 3S3TK)
WATER (UNII: 0 59 QF0 KO0 R)
ALO E VERA LEAF (UNII: ZY8 1Z8 3H0 X)
.ALPHA.-TO CO PHERO L ACETATE (UNII: 9 E8 X8 0 D2L0 )
PACKAG ING
#
ITEM CODE
PACKAGE DESCRIPTION
MARKETING START DATE
MARKETING END DATE
1
NDC:77731-0 0 5-0 1 2 in 1 PACKAGE
0 6 /17/20 20
1
10 0 0 mL in 1
                                
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