Dove

Manufacturer
Conopco Inc. d/b/a/ Unilever
Effective date
2024-10-24
Label type
HUMAN OTC DRUG LABEL
Version
7
Source
full-release
Hydrated at
2026-06-01 00:29:56

Label at a glance#

ProductDove
Active ingredientALCOHOL
Label structure10 sections

Indications and uses

• Hand sanitizer to help reduce bacteria on the skin

Label contents#

Full prescribing information#

DOVE NOURISHING HAND SANITIZER SHEA BUTTER & WARM VANILLA 8H MOISTURIZATION - Ethyl Alcohol gel

DESCRIPTION SECTION

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

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Ethyl Alcohol 61%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

• Hand sanitizer to help reduce bacteria on the skin

Warnings

WARNINGS SECTION

• For external use only
• Flammable. Keep away from fire or flame
• Avoid contact with eyes,
in case of contact, rinse eyes thoroughly with water immediately.
• If irritation develps, discontinue use and consult a doctor.

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.

Other information

OTHER SAFETY INFORMATION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Glycerin, Butylene Glycol, Dimethicone, Glycine Soja (Soybean) Oil, Fragrance (Parfum), Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Echium Plantagineum Seed Oil, Aminomethyl Propanol, Hydrogenated Lecithin, Tocopherol, Xanthan Gum, Stearic Acid, Citric Acid, Benzyl Alcohol, Coumarin, Hexyl Cinnamal, Limonene, Linalool .

Questions?

OTC - QUESTIONS SECTION

1-800-761-3683

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DoveHandSanitizerSheaButterDoveHandSanitizerSheaButter

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2289402ethanol 61 % Topical GelPSN7
2289402ethanol 0.61 ML/ML Topical GelSCD7
2289402ethanol 61 % Topical GelSY7

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
baf7f49c-75b6-496b-a00e-8e766a8e4f03Product name120210127
ebc62596-fc97-4d03-9483-7ba095d25db7Product name120151210
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
64942-1746-1Dove236 mL in 1 CONTAINERGEL2367
64942-1746-2Dove59 mL in 1 CONTAINERGEL597
64942-1746-3Dove1000 mL in 1 CONTAINERGEL10007

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
64942-1746DOVE (HAND SANITIZER SHEA BUTTER) GEL [CONOPCO INC. D/B/A/ UNILEVER]7Current NDC, Legacy NDC, 3 package rows20241027_a735d885-bacd-0f5c-e053-2a95a90ad14a.zip

Products#

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

DailyMed product names page 1 of 1 · 21 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
64942-174664942-1746-1, 64942-1746-2, 64942-1746-3

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 19 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 SHEA BUTTERConopco Inc. d/b/a/ Unilevera735d885-bacd-0f5c-e053-2a95a90ad14a2024-10-24WarningsExact identifier
ndc (package): 64942-1746-1
ndc (package): 64942-1746-2
ndc (package): 64942-1746-3
ndc (product): 64942-1746
ndc11 (package): 64942174603
ndc11 (package): 64942174602
ndc11 (package): 64942174601
spl id: 253c105b-215a-1e6e-e063-6294a90a11d7
spl set id: a735d885-bacd-0f5c-e053-2a95a90ad14a

Reported adverse events (FAERS/openFDA)#

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