Up & Up 849.001/849AA-AG rev 0, rev 1 & 849BA Moisturizing Hand Sanitizer

Alcohol by

Drug Labeling and Warnings

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

Drug Details [pdf]

ALCOHOL- alcohol liquid 
Target Corporation

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Up & Up 849.001/849AA-AG rev 0, rev 1 & 849BA
Moisturizing Hand Sanitizer

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

Questions?

1-800-910-6874

Claim

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

ADVERSE REACTION

Dist. by Target Corp., Mpls., MN 55403

Made in U.S.A. with U.S. and foreign components

TM & ©2020 Target Brands, Inc. 

Shop Target.com

DSP-TN-21091

DSP-MO-20087

DSP-MO-28

SDS-MO-20068

principal display panel

kills 99.99% of germs*

hand

sanitizer

up & up™

32 FL OZ (946.2 mL)

ALCOHOL 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11673-988
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 INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)
GLYCERIN (UNII: PDC6A3C0OX)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
TOCOPHEROL (UNII: R0ZB2556P8)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11673-988-16	59 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	04/29/2020	02/22/2026
2	NDC: 11673-988-34	236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	04/29/2020	02/16/2026
3	NDC: 11673-988-45	946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	04/29/2020	04/26/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	04/29/2020	05/11/2026

Labeler - Target Corporation (006961700)

Registrant - Nice-Pak Products, LLC (119091520)

Establishment
Name	Address	ID/FEI	Business Operations
Nice-Pak Products, LLC		119091514	manufacture(11673-988)

Establishment
Name	Address	ID/FEI	Business Operations
Nice-Pak Products, LLC		119091520	manufacture(11673-988)

Revised: 5/2026

Document Id: 518cdd38-ca36-41a0-e063-6294a90ad9fd

34390-5

Set id: 70943839-0fdf-49c7-9021-da5a081e9ea6

Version: 13

Effective Time: 20260511