365 Winterberry Hand Sanitizer Wipes

Manufacturer
Whole Foods Market, Inc.
Effective date
2025-10-09
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
monthly-update
Hydrated at
2026-06-03 17:38:54

Label at a glance#

Product365 Winterberry Hand Sanitizer Wipes
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

• for hand sanitizing to decrease bacteria on skin when water and soap are not avaliable • recommended for repeated use

Dosage and administration

• remove and unfold wipe •wet hands thoroughly with product and let air dry

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 65% v/v

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

• for hand sanitizing to decrease bacteria on skin when water and soap are not avaliable

• recommended for repeated use

Warnings

WARNINGS SECTION

For external use only.

Flammable keep away from fire or flame.

When using this product do not use in or near eyes, if contact occurs, flush thoroughly with water.

Stop use and contact a doctor if irritation or redness persists for more than 72 hours.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away

Directions

DOSAGE & ADMINISTRATION SECTION

• remove and unfold wipe

•wet hands thoroughly with product and let air dry

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aloe Barbadensis Leaf Extract
Althaea Officinalis Root Extract
Avena Sativa (Oat) Kernel Extract
Camellia Sinensis Leaf Extract
Chamomilla Recutita (Matricaria) Flower Extract
Cucumis Sativus (Cucumber) Fruit Extract
Glycerin

1Fragrance(natural)

Isopropyl alcohol

Water.

1 complies with iso 9235, see www.wholefoodsmarket.com form more information.

Questions, Comments?

OTC - QUESTIONS SECTION

1-844-WFM-TALK(1-844-936-8255)

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 42681-0034-1

365 WHOLE FOODS MARKET

REFRESHING WIPES

Hand Sanitizer

Winterberry

99.9% effective against most common germs*

Made without Benzalkonium Chloride

Limited Edition

PEEL & SEAL

10 WIPES

6IN x 7.5IN (15.25cm x 19.05cm)

DO NOT FLUSH

DISTRIBUTED BY: WHOLE FOODS MARKET

AUSTIN, TX 78703

2020 WHOLE FOODS MARKET IP, LP

www.wholefoodsmarket.com

WARNING: THESE WIPES CONTAIN ALCOHOL, WHICH CAN DISCOLOR SOME FABRICS AND SURFACES. ALWAYS TEST AN INCONSPICUOUS SPOT FIRST. DISCLAIMER: ALCOHOL EVAPORATES WITH TIME. TO KEEP THESE WIPES FRESH AND EFFECTIVE RESEAL SECURELY AFTER EACH USE AND STORE AT 75F OR BELOW. KEEP OUT OF DIRECT SUNLIGHT.

DISCARD AFTER USE. DO NOT FLUSH.

*ESCHERICHIA COLI, STAPHYLOCOCCUS AUREUS, SALMONELLA TYPHIMURIUM, PSEUDOMONAS AERUGINOSA, BURKHOLDERIA CEPACIA, ENTEROBACTER CLOACAE, ENTEROCOCCUS FAECALIS, STREPTOCOCCUS PYOGENES, CANDIDA ALBICANS, ASPERGILLUS BRASILIENSIS.

Made Without:

Benzalkonium Chloride, Parabens or Triclosan

Glycerin & Aloe Vera to replace moisture

99.9% effective against most common germs*

FSC MIX Paper

FSC C109834

UPC 099482510350

Seal LabelSeal Label

LABELLABEL

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1Product name120230829
3c386306-c48a-413e-bb69-70cb268496f3Product name120210727
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
42681-003442681-0034-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
42024-10-15full-release2026-06-01 00:25:30

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
4d607a5c-dbdd-ba3c-e063-6394a90ad30c03769aee-e0a0-96bf-e063-6294a90ac13f2026-03-19WarningsExact identifier
spl set id: 03769aee-e0a0-96bf-e063-6294a90ac13f

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.