FDA.reportPublic FDA data

Whole Foods 365 Lavender Hand Sanitizer Gel 1 fl oz

Manufacturer
Whole Foods Market, Inc. | KDC/ONE SOCAL LABORATORIES, LLC
Effective date
2024-11-02
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:33:33

Label at a glance#

ProductHand Sanitizer Lavender
Active ingredientALCOHOL
Label structure12 sections

Storage and handling

Other information do not store above 104°F (40°C).

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient

Ethyl Alcohol 62%

OTC - PURPOSE SECTION

Purpose

Antiseptic

WARNINGS SECTION

For external use only. Flammable. Keep away from fire or flame.

OTC - WHEN USING SECTION

When using this product avoid contact with eyes. If eye contact occurs, rinse with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if skin irritation or redness develops.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of accidental ingestion, seek medical help or contact a Poison Control Center immediately.

INDICATIONS & USAGE SECTION

Uses to help reduce bacteria on the skin

DOSAGE & ADMINISTRATION SECTION

Directions apply enough gel to wet hands and rub together until dry. Use 1 to 3 times daily.

STORAGE AND HANDLING SECTION

Other information do not store above 104°F (40°C).

OTC - QUESTIONS SECTION

Questions, Comments?

customer.questions@wholefoods.com

1-844-963-8255

INACTIVE INGREDIENT SECTION

Inactive ingredients water, isopropyl alcohol, hydroxyethylcellulose, salvia hispanica (chia) seed oil, glycerin, helianthus annuus (sunflower) seed oil, rosmarinus officinalis (rosemary) leaf extract, fragrance (natural), triethyl citrate.

*Complies with ISO 9235, see www.wholefoodsmarket.com for more information.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LHS1FPLHS1FPLHS1DFLHS1DF

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581660ethanol 62 % Topical GelPSN2
581660ethanol 0.62 ML/ML Topical GelSCD2
581660ethanol 62 % Topical GelSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
42681-0010-12024-11-03C16284748780-11030e365-1ad1-111a-e063-dadaa90a10e2Whole Foods 365 Lavender Hand Sanitizer Gel 1 fl oz
42681-0010-12024-01-30C16284748780-11030e365-1ad1-111a-e063-dadaa90a10e2Whole Foods 365 Lavender Hand Sanitizer Gel 1 fl oz

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
42681-0010-1Hand SanitizerLavender30 mL in 1 BOTTLE, PLASTICGEL302

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
42681-0010HAND SANITIZER LAVENDER (ETHYL ALCOHOL) GEL [WHOLE FOODS MARKET, INC.]2Current NDC, Legacy NDC, 1 package rows20241104_ec8c7597-a3f1-65a8-e053-2995a90a69a1.zip

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
42681-001042681-0010-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
POLYSORBATE 207T1F30V5YHIACT
ISOPROPYL ALCOHOLND2M416302IACT
WATER059QF0KO0RIACT
HYDROXYETHYL CELLULOSE (100 MPA.S AT 2%)R33S7TK2EPIACT
CHIA SEED OILMC2LH51BO7IACT
GLYCERINPDC6A3C0OXIACT
SUNFLOWER OIL3W1JG795YIIACT
ROSEMARYIJ67X351P9IACT
ALCOHOL3K9958V90MACTIB

Source Document#

Source XML

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
Hand Sanitizer LavenderETHYL ALCOHOLWhole Foods Market, Inc.ec8c7597-a3f1-65a8-e053-2995a90a69a12024-11-02WarningsExact identifier
ndc (package): 42681-0010-1
ndc (product): 42681-0010
ndc11 (package): 42681001001
spl id: 25f910c2-5ea8-ed23-e063-6394a90a1d5e
spl set id: ec8c7597-a3f1-65a8-e053-2995a90a69a1

Reported adverse events (FAERS/openFDA)#

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