Dove

Manufacturer
Conopco Inc. d/b/a/ Unilever
Effective date
2024-11-07
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:36:20

Label at a glance#

ProductDove
Active ingredientALCOHOL
Label structure11 sections

Indications and uses

• Hand sanitizer to help reduce bacteria on the skin. For use when soap and water are not available.

Dosage and administration

• Wet hands thoroughly with product and rub lightly until dry.

Label contents#

Full prescribing information#

DOVE MOISTURIZING HAND SANITIZER WIPES SHEA BUTTER & WARM VANILLA SCENT - ethyl alcohol cloth

DESCRIPTION SECTION

Dove Nourishing Hand Sanitizer Shea Butter & Warm Vanilla 8h Moisturization

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Ethyl Alcohol 76%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

• Hand sanitizer to help reduce bacteria on the skin. For use when soap and water are not available.

Warnings

WARNINGS SECTION

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

Do not store in car.
Do not use in children less than 12 months of age
Do not use on open skin wounds
When using this product, do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water
Stop use and ask doctor if irritation or redness develop

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

• Keep out of reach of children except under adult supervision.

If swallowed, get medical help or contact a poison control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

• Wet hands thoroughly with product and rub lightly until dry.

Other information

OTHER SAFETY INFORMATION

• Avoid excessive heat. Store below 105˚F (40˚C).
• May discolor fabrics or surfaces.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Glycerin, Butylene Glycol, Fragrance (Parfum), Niacinamide, Tocopheryl Acetate, Stearic Acid, Tetrasodium EDTA, Coumarin, Hexyl Cinnamal, Limonene, Linalool.

Questions?

OTC - QUESTIONS SECTION

1-800-761-3683

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Dove Sanitizer Wipes SheaDove Sanitizer Wipes Shea

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2397694ethanol 76 % Medicated PadPSN2
2397694ethanol 0.76 ML/ML Medicated PadSCD2
2397694ethanol 76 % Medicated PadSY2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
64942-2041-1Dove8.57 mL in 1 APPLICATORCLOTH8.572
64942-2041-2Dove20 in 1 POUCHCLOTH202
64942-2041-3Dove8.57 mL in 1 APPLICATORCLOTH8.572
64942-2041-4Dove40 in 1 POUCHCLOTH402

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
64942-2041DOVE (HAND SANITIZER WIPES SHEA BUTTER AND WARM VANILLA SCENT) CLOTH [CONOPCO INC. D/B/A/ UNILEVER]2Current NDC, Legacy NDC, 4 package rows20241109_df73e518-caec-a73b-e053-2995a90a69f5.zip

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
64942-204164942-2041-1, 64942-2041-2, 64942-2041-3, 64942-2041-4

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

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
DoveHAND SANITIZER WIPES SHEA BUTTER AND WARM VANILLA SCENTConopco Inc. d/b/a/ Unileverdf73e518-caec-a73b-e053-2995a90a69f52024-11-07WarningsExact identifier
ndc (package): 64942-2041-4
ndc (package): 64942-2041-3
ndc (package): 64942-2041-2
ndc (package): 64942-2041-1
ndc (product): 64942-2041
ndc11 (package): 64942204104
ndc11 (package): 64942204102
ndc11 (package): 64942204101
ndc11 (package): 64942204103
spl id: 2657427b-0229-8bac-e063-6394a90aff48
spl set id: df73e518-caec-a73b-e053-2995a90a69f5

Reported adverse events (FAERS/openFDA)#

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