HAND SANITIZER- ethyl alcohol spray

Hand Sanitizer by

Drug Labeling and Warnings

Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by L&R Distributors, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Ethyl Alcohol 74% V/V

INDICATIONS & USAGE

• For hand washing to decrease bacteria on the skin
• recommended for repeated use throughout the day

PUPOSE

ANTISEPTIC

WARNINGS

For external use only
Flammable. Keep away from fire or flame.
When using this product avoid contact with the eyes. In case of contact, flush eyes thoroughly with water.
Stop use and contact a doctor if irritation or redness develop or lasts 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 - allow to dry without wiping - supervise children under 6 years old - not recommended for infants

OTHER INFORMATION

may discolor certain fabrics - store at room temperature 20°-25°C (66°-77°F).

INACTIVE INGREDIENTS

Water, Glycerin, Lavendula Angustifolia (Lavender) Oil, Tocopheryl Acetate, Aloe Barbadensis (Aloe Vera) Leaf Juice, Aloe Barbadensis Leaf Extract, Althaea Officinalis Root Extract, Centella Asiatica Extract, Chamomilla Recutita (Matricaria) Flower Extract, Citrus Aurantium Dulcis (Orange) Peel Extract, Citrus Grandis (Grapefruit) Fruit Extract, Citrus Limon (Lemon) Peel Extract, Cymbopogon Schoenanthus Leaf/Stem Extract, Equisetum Arvense Extract, Humulus Lupulus (Hops) Extract, Rosmarinus Officinalis (Rosemary) Leaf Extract, Salvia Sclarea (Clary) Extract, Vaccinium Myrtillus Fruit/Leaf Extract, Yucca Schidigera Leaf/Root/Stem Extract.

PRINCIPAL DISPLAY PANEL

NDC: 15127-008-02

INGREDIENTS AND APPEARANCE

HAND SANITIZER 
ethyl alcohol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 15127-008
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	74 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
LEMON PEEL (UNII: 72O054U628)
EQUISETUM ARVENSE WHOLE (UNII: 73DM367W4P)
GRAPEFRUIT PEEL (UNII: 3582N05Q44)
VACCINIUM MYRTILLUS WHOLE (UNII: EE76EZ4QNZ)
SALVIA SCLAREA WHOLE (UNII: I0440F92M2)
ORANGE PEEL (UNII: TI9T76XD44)
CYMBOPOGON SCHOENANTHUS WHOLE (UNII: RJJ0F54DE8)
YUCCA SCHIDIGERA (UNII: 08A0YG3VIC)
GLYCERIN (UNII: PDC6A3C0OX)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
CENTELLA ASIATICA (UNII: 7M867G6T1U)
CHAMOMILE (UNII: FGL3685T2X)
WATER (UNII: 059QF0KO0R)
ALTHAEA OFFICINALIS ROOT (UNII: TRW2FUF47H)
LAVENDER OIL (UNII: ZBP1YXW0H8)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
HUMULUS LUPULUS WHOLE (UNII: 912A6Q1N4A)
ROSMARINUS OFFICINALIS WHOLE (UNII: EA3289138M)

Product Characteristics
Color		Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 15127-008-02	59 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	12/02/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	12/02/2024

Labeler - L&R Distributors, Inc. (012578514)