ETHYL ALCOHOL liquid

Drug Labeling and Warnings

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 external 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 105°F
• may discolor some fabrics
• harmful to wood finishes and plastics

Inactive ingredients

water, carbomer, fragrance, glycerin, isopropyl myristate, blue 1

Questions?

1-866-694-3769

Claim

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

Adverse Reaction

Distributed by: UpLift Brands, LLC

St. Louis, MO 63114

www.germx.com

Principal Display Panel

germ X ®

SINCE 1997

ORIGINAL

HAND SANITIZER

OCEAN BREEZE

Kills 99.99% of Germs*

2 FL OZ (59 mL)

INGREDIENTS AND APPEARANCE

ETHYL ALCOHOL 
ethyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83986-471
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)
GLYCERIN (UNII: PDC6A3C0OX)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83986-471-16	59 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	04/24/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	04/24/2026

Labeler - UpLift Brands, LLC  (119091527)

Registrant - Nice-Pak Products, LLC (119091520)

Establishment
Name	Address	ID/FEI	Business Operations
Nice-Pak Products, LLC		119091514	manufacture(83986-471)