Vaseline Clinical Care Hand Sanitizer Lotion

Manufacturer
Conopco Inc. d/b/a/ Unilever
Effective date
2024-10-24
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 00:29:59

Label at a glance#

ProductVaseline
Active ingredientBENZALKONIUM CHLORIDE
Label structure10 sections

Indications and uses

helps decrease bacteria on the hands

Dosage and administration

Apply product thoroughly to hands. Rub hands together until absorbed. Do not wipe off or rinse. Apply to hands as needed.

Label contents#

Full prescribing information#

VASELINE CLINICAL CARE HAND SANITIZER LOTION - Benzalkonium Chloride lotion

DESCRIPTION SECTION

Vaseline Clinical Care Hand Sanitizer Lotion

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antibacterial

Uses

INDICATIONS & USAGE SECTION

helps decrease bacteria on the hands

Warnings

WARNINGS SECTION

For external use only
Avoid contact with eyes,
In case of contact, rinse eyes thoroughly with water.
If irritation develops, 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.

Directions

DOSAGE & ADMINISTRATION SECTION

Apply product thoroughly to hands. Rub hands together until absorbed. Do not wipe off or rinse. Apply to hands as needed.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Glycerin, Tapioca Starch, Polyquaternium-37, Dicaprylyl Carbonate, Phenoxyethanol, Caprylyl Glycol, Fragrance (Parfum), Lauryl Glucoside, Tocopheryl Acetate, Citronellol, Limonene, Linalool, Titanium Dioxide (CI 77891)

Questions or Comments?

OTC - QUESTIONS SECTION

1-800-457-7964

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Vaseline Hand Sanitizer LotionVaseline Hand Sanitizer LotionPackaging

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1046442benzalkonium chloride 0.13 % Topical LotionPSN4
1046442benzalkonium chloride 1.3 MG/ML Topical LotionSCD4
1046442benzalkonium chloride 0.13 % Topical LotionSY4

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
64942-1849-1Vaseline88.5 mL in 1 TUBELOTION88.54
64942-1849-2Vaseline150 mL in 1 TUBELOTION1504
64942-1849-4Vaseline236 mL in 1 BOTTLE, PUMPLOTION2364

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
64942-1849VASELINE (CLINICAL CARE HAND SANITIZER LOTION) LOTION [CONOPCO INC. D/B/A/ UNILEVER]4Current NDC, Legacy NDC, 3 package rows20241027_ba0aa323-8887-597f-e053-2995a90a2077.zip

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
64942-184964942-1849-1, 64942-1849-2, 64942-1849-4

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 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
VaselineCLINICAL CARE HAND SANITIZER LOTIONConopco Inc. d/b/a/ Unileverba0aa323-8887-597f-e053-2995a90a20772024-10-24WarningsExact identifier
ndc (package): 64942-1849-4
ndc (package): 64942-1849-2
ndc (package): 64942-1849-1
ndc (product): 64942-1849
ndc11 (package): 64942184904
ndc11 (package): 64942184902
ndc11 (package): 64942184901
spl id: 253c45b5-1227-9ed6-e063-6394a90a9cb4
spl set id: ba0aa323-8887-597f-e053-2995a90a2077

Reported adverse events (FAERS/openFDA)#

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