HAND SANITIZER LAVENDER- ethyl alcohol gel

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

Ethyl Alcohol 62%

PURPOSE

Purpose

Antiseptic

WARNINGS

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

WHEN USING

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

STOP USE

Stop use and ask a doctor ifskin 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.

INDICATIONS & USAGE

Usesto help reduce bacteria on the skin

DOSAGE & ADMINISTRATION

Directionsapply enough gel to wet hands and rub together until dry. Use 1 to 3 times daily.

STORAGE AND HANDLING

Other informationdo not store above 104°F (40°C).

QUESTIONS

Questions, Comments?

customer.questions@wholefoods.com

1-844-963-8255

INACTIVE INGREDIENT

Inactive ingredientswater, isopropyl alcohol, hydroxyethylcellulose, salvia hispanica (chia) seed oil, glycerin, helianthus annuus (sunflower) seed oil, rosmarinus officinalis (rosemary) leaf extract, fragrance (natural)*, polysorbate 20.

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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

HAND SANITIZER  LAVENDER
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 42681-7162
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
WATER (UNII: 059QF0KO0R)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
HYDROXYETHYL CELLULOSE (100 MPA.S AT 2%) (UNII: R33S7TK2EP)
CHIA SEED OIL (UNII: MC2LH51BO7)
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: 42681-7162-2	946 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	10/09/2023

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(42681-7162)