HAND SANITIZER CUCUMBER ALOE- ethyl alcohol spray

Hand Sanitizer by

Drug Labeling and Warnings

Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Whole Foods Market, Inc., V Manufacturing Logistics, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient Purpose

Ethyl Alcohol 62% Antiseptic

PURPOSE

Uses ■ to help reduce bacteria on the skin.

WARNINGS

For external use only. Flammable. Keep away from fire or flame.

WHEN USING

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

STOP USE

Stop use and ask a doctor if skin irritation or redness develops.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. In case of accidental ingestion, seek medical help or contact a Poison Control Center immediately.

DOSAGE & ADMINISTRATION

Directions ■ apply 1 to 2 sprays on hands and rub together until dry.

INDICATIONS & USAGE

STORAGE AND HANDLING

Other information ■ do not store above 104°F (40°C).

INACTIVE INGREDIENT

Inactive ingredients water, isopropyl alcohol, glycerin, fragrance (natural)*, helianthus annuus (sunflower) seed oil, rosmarinus officinalis (rosemary) leaf extract, triethyl citrate.

*Complies with ISO 9235, see www.wholefoodsmarket.com for more information.

QUESTIONS

Questions, Comments? ■ customer.questions@wholefoods.com ■ 1-844-936-8255

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

HAND SANITIZER  CUCUMBER ALOE
ethyl alcohol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 42681-0009
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
TRIETHYL CITRATE (UNII: 8Z96QXD6UM)
WATER (UNII: 059QF0KO0R)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
GLYCERIN (UNII: PDC6A3C0OX)
SUNFLOWER OIL (UNII: 3W1JG795YI)
ROSEMARY (UNII: IJ67X351P9)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 42681-0009-1	59 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/01/2020	12/31/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	01/01/2020	12/31/2024

Labeler - Whole Foods Market, Inc. (196175616)

Registrant - V Manufacturing Logistics, Inc. (825176857)