HAND SANITIZER LAVENDER- 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., KDC/ONE SOCAL LABORATORIES, LLC. 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, polysorbate 20.

*Complies within 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  LAVENDER
ethyl alcohol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 42681-0006
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
ISOPROPYL ALCOHOL (UNII: ND2M416302)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
SUNFLOWER OIL (UNII: 3W1JG795YI)
ROSEMARY (UNII: IJ67X351P9)
POLYSORBATE 20 (UNII: 7T1F30V5YH)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 42681-0006-2	59 mL in 1 BOTTLE; Type 0: Not a Combination Product	10/09/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	01/01/2020

Labeler - Whole Foods Market, Inc. (196175616)

Registrant - KDC/ONE SOCAL LABORATORIES, LLC (118384240)

Establishment
Name	Address	ID/FEI	Business Operations
KDC/ONE SOCAL LABORATORIES, LLC		118384240	manufacture(42681-0006)