HAND SANITIZER PUMPKIN CARDAMOM- 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., V Manufacturing & Logistics, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient 

Ethyl Alcohol 62% v/v

PURPOSE

Purpose     

Antiseptic

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.

INDICATIONS & USAGE

Uses to help reduce bacteria on the skin

DOSAGE & ADMINISTRATION

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

STORAGE AND HANDLING

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

QUESTIONS

Questions, Comments?

customer.questions@wholefoods.com

1-844-963-8255

INACTIVE INGREDIENT

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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

HAND SANITIZER  PUMPKIN CARDAMOM
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 42681-7422
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)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 42681-7422-1	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/21/2018	09/30/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	02/01/2018	09/30/2020

Labeler - Whole Foods Market, Inc. (196175616)

Registrant - V Manufacturing & Logistics, Inc. (079081508)