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 00:36:19

Label at a glance#

ProductDove
Active ingredientALCOHOL
Label structure10 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. Do not wipe off or rinse.

Label contents#

Full prescribing information#

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. 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 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. Do not wipe off or rinse.

Other information

OTHER SAFETY INFORMATION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Glycerin, Glycine Soja (Soybean) Oil, Butylene Glycol, Dimethicone, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Fragrance (Parfum), Aminomethyl Propanol, Stearic Acid, Palmitic Acid, Benzyl Alcohol.

Questions?

OTC - QUESTIONS SECTION

1-800-761-3683

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Dove Hand Sanitizer SenssitiveDove Hand Sanitizer Senssitive

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2289402ethanol 61 % Topical GelPSN2
2289402ethanol 0.61 ML/ML Topical GelSCD2
2289402ethanol 61 % Topical GelSY2

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
64942-2035-1Dove236 mL in 1 CONTAINERGEL2362
64942-2035-2Dove59 mL in 1 CONTAINERGEL592

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
64942-2035DOVE (NOURISHING HAND SANITIZER SENSITIVE SKIN 8HR MOISTURIZATION) GEL [CONOPCO INC. D/B/A/ UNILEVER]2Current NDC, Legacy NDC, 2 package rows20241109_ddcbab1c-7af9-2656-e053-2995a90ad07a.zip

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
64942-203564942-2035-1, 64942-2035-2

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

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
DoveNOURISHING HAND SANITIZER SENSITIVE SKIN 8HR MOISTURIZATIONConopco Inc. d/b/a/ Unileverddcbab1c-7af9-2656-e053-2995a90ad07a2024-11-07WarningsExact identifier
ndc (package): 64942-2035-1
ndc (package): 64942-2035-2
ndc (product): 64942-2035
ndc11 (package): 64942203501
ndc11 (package): 64942203502
spl id: 26574d45-52e3-7e63-e063-6394a90ab334
spl set id: ddcbab1c-7af9-2656-e053-2995a90ad07a

Reported adverse events (FAERS/openFDA)#

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