Kroger Comforts 523.000/523AA Hand Sanitzer

Hand Sanitizer by

Drug Labeling and Warnings

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

Drug Details [pdf]

HAND SANITIZER- ethyl alcohol gel 
The Kroger Co

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Kroger Comforts 523.000/523AA
Hand Sanitzer

Active ingredient

Ethyl alcohol 65%

Purpose

Antispetic

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 heat and 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

• skin 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 abut 105 °F.
• May discolor some fabrics
• Harmful to wood finishes and plastics

Inactive ingredients

aloe barbadensis leaf juice, benzophenone-4, blue 1, carbomer, fragrance, glycerin, isopropyl myristate, propylene glycol, red 33, tocopheryl acetate, water

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

Made in the USA with US and foreign components.

Distributed by The Kroger Co.

Cincinnati, Ohio 45202

www.comfortsforbaby.com

principal display panel

Comforts

Hand Sanitizer

Lavender & Chamomile Scent

• Kills 99.99 of germs*

8 FL OZ (236 mL)

HAND SANITIZER 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 30142-523
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	65 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
SULISOBENZONE (UNII: 1W6L629B4K)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
GLYCERIN (UNII: PDC6A3C0OX)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 30142-523-34	236 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	08/19/2010	10/23/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	08/19/2010	10/23/2021

Labeler - The Kroger Co (006999528)

Registrant - Consumer Product Partners, LLC (119091520)

Establishment
Name	Address	ID/FEI	Business Operations
Consumer Product Partners, LLC		119091514	manufacture(30142-523)

Revised: 10/2024

Document Id: 2516b257-aec1-aa1e-e063-6394a90ab092

34390-5

Set id: 15f9c4b4-1d71-4379-90cb-123007d2de25

Version: 4

Effective Time: 20241022