Ethyl Alcohol by DOLLAR GENERAL CORPORATION / Vi Jon, LLC ETHYL ALCOHOL liquid

Ethyl Alcohol by

Drug Labeling and Warnings

Ethyl Alcohol by is a Otc medication manufactured, distributed, or labeled by DOLLAR GENERAL CORPORATION, Vi Jon, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Ethyl Alcohol 62%

Purpose

Antiseptic

Uses

• 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 thoroughly 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 or acrylates/C10-30 alkyl acrylate crosspolymer, fragrance, glycerin, isopropyl myristate, tocopheryl acetate

Claim

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

ADVERSE REACTIONS SECTION

100% Satisfaction Guaranteed! (888)309-9030

DISTRIBUTED BY OLD EAST MAIN CO.

100 MISSION RIDGE

GOODLETTSVILLE, TN 37072

DSP-TN-21091 DSP-MO-20087

Principal display panel

STUDIO SELECTION ®

moisturizing

HAND SANITIZER

original

• With Vitamin E
• kills 99.99% of germs & bacteria*

32 FL OZ (1 QT) 946 mL

Principal display panel

Since 1903

Rexall™

Moisturizing

Hand Sanitizer

Kills 99.99% of Germs*

enriched with moisturizers

32 FL. OZ. (1QT) (946 mL)

INGREDIENTS AND APPEARANCE

ETHYL ALCOHOL 
ethyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75712-849
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)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
GLYCERIN (UNII: PDC6A3C0OX)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
TOCOPHEROL (UNII: R0ZB2556P8)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75712-849-34	236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	05/01/2023
2	NDC: 75712-849-16	59 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	05/01/2023
3	NDC: 75712-849-45	946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	05/01/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	05/01/2023

Labeler - DOLLAR GENERAL CORPORATION (006946172)

Registrant - Consumer Product Partners, LLC (119091520)

Establishment
Name	Address	ID/FEI	Business Operations
Consumer Product Partners, LLC		119091520	manufacture(75712-849)

Establishment
Name	Address	ID/FEI	Business Operations
Consumer Product Partners, LLC		119091514	manufacture(75712-849)