FDA.reportPublic FDA data

Whole Foods 365 Mojito MInt Hand Sanitizer Spray 2 fl oz

Manufacturer
Whole Foods Market, Inc. | V Manufacturing & Logistics, Inc.
Effective date
2020-02-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:42:06

Label at a glance#

ProductHand Sanitizer Mojito Mint
Active ingredientALCOHOL
Label structure11 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 Purpose

Organic Ethyl Alcohol 62% Antiseptic

OTC - PURPOSE SECTION

Uses ■ to help reduce bacteria on the skin.

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.

DOSAGE & ADMINISTRATION SECTION

Directions ■ apply 1 to 2 sprays on hands and rub together until dry

STORAGE AND HANDLING SECTION

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

INACTIVE INGREDIENT SECTION

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

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

OTC - QUESTIONS SECTION

Questions, Comments? ■ customer.questions@wholefoods.com ■ 1-844-936-8255

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Mojito Mint SprayMojito Mint Spray

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
42681-000842681-0008-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
TRIETHYL CITRATE8Z96QXD6UMIACT
WATER059QF0KO0RIACT
ISOPROPYL ALCOHOLND2M416302IACT
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
9d89e245-7069-fe1d-e053-2995a90ab4209d8a610f-1f80-0e54-e053-2a95a90a35e72020-02-01WarningsExact identifier
spl id: 9d89e245-7069-fe1d-e053-2995a90ab420
spl set id: 9d8a610f-1f80-0e54-e053-2a95a90a35e7

Reported adverse events (FAERS/openFDA)#

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