FRESH SCENT HAND SANITIZER- ethyl alcohol liquid

FRESH SCENT HAND SANITIZER by

Drug Labeling and Warnings

FRESH SCENT HAND SANITIZER by is a Otc medication manufactured, distributed, or labeled by GL 360. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

ACTIVE INGREDIENT

Active ingredients  

Ethyl Alcohol 62.0%

PURPOSE

Purpose  

Antimicrobial

INDICATIONS & USAGE

Use hand sanitizer
to help reduce
bacteria on skin.

WARNINGS

Flammable  Keep

away from heat and flame

WHEN USING

When using this
product avoid contact
with eyes. If contact
occurs, rinse
thoroughly with water.

STOP USE

Stop use and ask
doctor if irritation or
redness develops.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach
of children.
If swallowed, get
medical help or
contact a Poison
Control center
right away.

DOSAGE & ADMINISTRATION

Directions
■ Wet hands
thoroughly with
product and rub
into skin until dry.
■ Children under
6 years of age
should be
supervised by an
adult when using.

INACTIVE INGREDIENT

Inactive
Ingredients
Water (Aqua), Aloe
Barbadensis Leaf
Juice, Carbomer,
Fragrance, Glycerin,
Propylene Glycol,
Triethanolamine,
Tocopheryl Acetate.

Principal Display Package

FRESH SCENT
HAND SANITIZER
1 FL OZ (29 mL)

PEEL UP TO SEE
ADDITIONAL DRUG FACTS▼

Distributed By:
GL360, LLC
Troy Michigan, 48084
Made in China

↓Product Package↓

3 29500 00196 7

3 29500 00195 0

3 29500 00003 8

                               FRESH SCENT HAND SANITIZER by GL360, LLC

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INGREDIENTS AND APPEARANCE

FRESH SCENT HAND SANITIZER 
ethyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 29500-9823
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	17.98 mL  in 29 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
TROLAMINE (UNII: 9O3K93S3TK)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 29500-9823-1	29 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	01/01/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	01/01/2019

FRESH SCENT HAND SANITIZER 
ethyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 29500-9824
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	17.98 mL  in 29 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
TROLAMINE (UNII: 9O3K93S3TK)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 29500-9824-1	29 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	01/01/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	01/01/2019

FRESH SCENT HAND SANITIZER 
ethyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 29500-9825
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	17.98 mL  in 29 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
TROLAMINE (UNII: 9O3K93S3TK)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 29500-9825-1	29 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	01/01/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	01/01/2019

Labeler - GL 360 (966155082)