ALCOHOL liquid

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:

United Natural Foods, Inc. dba UNFI

Administration route:

TOPICAL

Prescription type:

OTC DRUG

Therapeutic indications:

Antiseptic - to decrease bacteria on the skin that could cause disease - recommended for repeated use - irritation and redness develop - condition persists for more than 72 hours

Authorization status:

OTC monograph not final

Summary of Product characteristics

                                ALCOHOL- ALCOHOL LIQUID
UNITED NATURAL FOODS, INC. DBA UNFI
----------
EQUALINE 826.000/826AA REV 1
MOISTURIZING HAND SANITIZER WITH ALOE
ACTIVE INGREDIENT
Ethyl Alcohol 62%
PURPOSE
Antiseptic
USES
to decrease bacteria on the skin that could cause disease
recommended for repeated use
WARNINGS
FOR EXTERNAL USE ONLY: HANDS
FLAMMABLE, KEEP AWAY FROM FIRE OR FLAME
WHEN USING THIS PRODUCT
keep out of eyes. In case of contact with eyes, flush thoroughly with
water
aoid contact with broken skin
do not inhale of ingest
STOP USE AND ASK A DOCTOR IF
irritation and redness develop
condition persists for more than 72 hours
KEEP OUT OF REACH OF CHILDREN.
If swallowed, get medical help or contact a Poison Control Center
right away.
DIRECTIONS
wet hands thoroughly with product and allow to dry without wiping
for children under 6, use only under adult supervision
not recommended for infants
OTHER INFORMATION
Do not store above 105° F
may discolor some fabrics
harmful to wood finishes and plastics
INACTIVE INGREDIENTS
water, carbomer, fragrance, glycerin, isopropyl myristate, Aloe
barbadensis leaf juice,
tocopheryl acetate, blue 1, yellow 5
ADVERSE REACTION
Like it or let us make it right.
That's our quality promise.
855-423-2630
DISTRIBUTED BY UNFI
PROVIDENCE, RI 02968 USA
PRINCIPAL DISPLAY PANEL
EQUALINE
MOISTURIZING
Hand Sanitizer
with Aloe and Vitamine E
2 FL OZ (59 mL)
ALCOHOL
alcohol liquid
PRODUCT INFORMATION
PRODUCT TYPE
HUMAN OTC DRUG
ITEM CODE (SOURCE)
NDC:41163-826
ROUTE OF ADMINISTRATION
TOPICAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRENGTH
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)
ALCOHOL
62 mL in 100 mL
INACTIVE INGREDIENTS
INGREDIENT NAME
STRENGTH
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII:
59TL3WG5CO)
GLYCERIN (UNII: PDC6A3C0OX)
TOCOPHEROL (UNII: R0ZB2556P8)
WATER (UNII: 059QF0KO0R)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
ALOE (UNII: V5VD430YW9)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
PACKAGING
# ITEM CODE
PACKAGE DESCRIP
                                
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