Sea and Ski Hand Sanitizer Gel

Manufacturer
Cross Brands Contract Filling
Effective date
2021-02-19
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:38:19

Label at a glance#

ProductSea and Ski Hand Sanitizer Gel
Active ingredientALCOHOL
Label structure8 sections

Indications and uses

To decrease bacteria on the skin that could cause disease Recommended for repeated use

Dosage and administration

wet hands thoroughly with product and allow to dry without wiping for children under 6, use only under adult supervision not recommended for infants

Storage and handling

do not store above 105°F may discolor some fabrics harmful to wood finishes and plastics

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Active IngredientActive IngredientEthyl Alcohol 62%

Purpose

OTC - PURPOSE SECTION

Purpose SectionPurpose SectionAntiseptic

Uses

INDICATIONS & USAGE SECTION

UsesUses

To decrease bacteria on the skin that could cause disease

Recommended for repeated use

Warnings

WARNINGS SECTION

WarningsWarnings

For external use only: Hands

Flammable, keep away from fire or flame

When Using

OTC - WHEN USING SECTION

When usingWhen usingWhen using this product keep out of eyes. In case of contact with eyes, flush thoroughly with water. Avoid contact with broken skin. Do not inhale or ingest

Stop use

OTC - STOP USE SECTION

Stop useStop useStop Use and ask a doctor if irritation or redness develops condition persists for more than 72 hours

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of childrenKeep out of reach of children

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

DirectionsDirectionswet hands thoroughly with product and allow to dry without wiping for children under 6, use only under adult supervision not recommended for infants

Other information

STORAGE AND HANDLING SECTION

Other informationOther informationdo not store above 105°F may discolor some fabrics harmful to wood finishes and plastics

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Inactive ingredientsInactive ingredients

acrylates copolymer*, aloe barbadensis leaf extract carbomer*, tocopheryl acetate (vitamin E), triethanolamine, water

*contains one or more of these ingredients

Package Label Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Front LabelFront Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581660ethanol 62 % Topical GelPSN2
581660ethanol 0.62 ML/ML Topical GelSCD2
581660ethanol 62 % Topical GelSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73440-2159-12023-01-30C16284748780-1f386c64a-382f-0266-e053-dadaa90a7c1aSea & Ski Advance Hand Sanitizer Gel 16oz

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73440-2159-1Sea and Ski Hand Sanitizer Gel416.24 g in 1 BOTTLE, PUMPGEL416.242

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73440-2159SEA AND SKI HAND SANITIZER GEL (ETHYL ALCOHOL) GEL [CROSS BRANDS CONTRACT FILLING]2Legacy NDC, 1 package rows20210220_bafeadef-d898-335c-e053-2a95a90ab0a3.zip

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73440-215973440-2159-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
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
bbb37a5e-cef4-ab51-e053-2a95a90ae655bafeadef-d898-335c-e053-2a95a90ab0a32021-02-19WarningsExact identifier
spl id: bbb37a5e-cef4-ab51-e053-2a95a90ae655
spl set id: bafeadef-d898-335c-e053-2a95a90ab0a3

Reported adverse events (FAERS/openFDA)#

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