Alcohol by H-E-B / Vi Jon, LLC / Vi-Jon, LLC ALCOHOL liquid

Alcohol by

Drug Labeling and Warnings

Alcohol by is a Otc medication manufactured, distributed, or labeled by H-E-B, Vi Jon, LLC, Vi-Jon, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Ethyl Alcohol 62%

Purpose

Antiseptic

Uses

• for handwashing to decrease bacteria on the skin that could cause disease
• recommended for repeated use

Warnings

For exterenal use only-hands

Flammable, keep away from fire or flame.

When using this product

• keep out of eyes.  In case of contact with eyes, flush thoroghly with water.
• avoid contact with broken skin
• do not inhale or ingest

Stop use and ask a doctor if

• irritation and redness develop
• condition persists 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 and allow to dry without wiping
• for children under 6, use only under adult supervision
• not recommended for infants

Other information

• do not store above 105⁰F
• may discolor some fabrics
• harmful to wood finishes and plastics

Inactive ingredients

water, carbomer, fragrance, glycerin, isopropyl myristate, Aloe barbadensis leaf juice, tocopheryl acetate, blue 1, yellow 5

Questions?

1-888-287-1915

SPL UNCLASSIFIED SECTION

*Effective at eliminating 99.99% of many common harmful germs and bacteria in as little as 15 seconds.

SDS-MO-15036 SDA-WI-2486 DSP-MO-28 DSP-MO-34

DISTRIBUTED BY: H-E-B, SAN ANTONIO, TX 748204

PRINCIPAL DISPLAY PANEL

HILL COUNTRY FARE

HAND 

SANITIZER

WITH ALOE

KILLS 99.99% OF GERMS

12 FL OZ (354 mL)

INGREDIENTS AND APPEARANCE

ALCOHOL 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 37808-826
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	62 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
GLYCERIN (UNII: PDC6A3C0OX)
TOCOPHEROL (UNII: R0ZB2556P8)
WATER (UNII: 059QF0KO0R)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
ALOE (UNII: V5VD430YW9)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 37808-826-32	355 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/19/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	07/19/2019

Labeler - H-E-B (007924756)

Registrant - Vi Jon, Inc. (088520668)

Establishment
Name	Address	ID/FEI	Business Operations
Vi Jon, Inc.		088520668	manufacture(37808-826)

Establishment
Name	Address	ID/FEI	Business Operations
Vi Jon, Inc		150931459	manufacture(37808-826)