HAND SANITIZER- alcohol liquid

Hand Sanitizer by

Drug Labeling and Warnings

Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Uline, Vi-Jon, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Ethyl alcohol 70%

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 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, PEG-8 Dimethicone, meadowfoamamidopropyl betaine, glyceryl caprylate/caprate, glycerin, tocopheryl acetate, isopropyl Myristate

ADVERSE REACTION

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

Distributed by: ULINE

12575 Uline Drive, Pleasant Prairied, WI 53158

1-800-295-5510  uline.com

DSP-TN-21091 DSP-MO-20087 DSP-MO-28 SDS-MO-20068

principal display panel

ULINE

Foaming

Hand Samitizer

Kills 99.99% of germs instantly*

S-24121

18 FL OZ (532 mL)

INGREDIENTS AND APPEARANCE

HAND SANITIZER 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69790-456
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
PEG-8 DIMETHICONE (UNII: GIA7T764OD)
MEADOWFOAMAMIDOPROPYL BETAINE (UNII: HNV0L650LG)
GLYCERYL CAPRYLATE/CAPRATE (UNII: G7515SW10N)
GLYCERIN (UNII: PDC6A3C0OX)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69790-456-44	532 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	12/08/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	12/08/2020

Labeler - Uline (039612668)

Registrant - Consumer Product Partners, LLC (119091520)

Establishment
Name	Address	ID/FEI	Business Operations
Consumer Product Partners, LLC		119091520	manufacture(69790-456)