Sea and Ski Advance Hand Sanitizer

Manufacturer
Cross-Brands Contract Filling | Cross Brands Contract Filling
Effective date
2021-02-19
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:38:18

Label at a glance#

ProductSea and Ski Advance Hand Sanitizer
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 ony under adult supervision not recommeded 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 Ingredient

Ethyl alcohol 62%

Purpose

OTC - PURPOSE SECTION

PurposePurpose

Antispetic

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 - DO NOT USE 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 childrenKeep 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 ony under adult supervision not recommeded 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 ingredientsacrylates copolymer*, aloe barbadensis leaf extract, carbomer*, tocopheryl acetate (vitamin E), triethanolamine, water

*contains one or more of these ingredients

Package Label- Principle Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Package Label- Principle Display PanelPackage Label- Principle Display Panel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581660ethanol 62 % Topical GelPSN3
581660ethanol 0.62 ML/ML Topical GelSCD3
581660ethanol 62 % Topical GelSY3

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73440-3130-12023-01-30C16284748780-1f386c64a-228b-0266-e053-dadaa90a7c1aSea&Ski Advance Hand Sanitizer 128oz
73440-3130-22023-01-30C16284748780-1f386c64a-228b-0266-e053-dadaa90a7c1aSea&Ski Advance Hand Sanitizer 128oz

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73440-3130-1Sea and Ski Advance Hand Sanitizer3779.78 g in 1 BOTTLE, PUMPGEL3779.783
73440-3130-2Sea and Ski Advance Hand Sanitizer3779.78 g in 1 BOTTLE, PUMPGEL3779.783

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73440-3130SEA AND SKI ADVANCE HAND SANITIZER (ETHYL ALCOHOL) GEL [CROSS-BRANDS CONTRACT FILLING]3Legacy NDC, 2 package rows20210220_a6a4c642-1c50-56c5-e053-2a95a90ae319.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
73440-313073440-3130-1, 73440-3130-2

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
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT

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
bbb3120e-d3f8-51e7-e053-2995a90a3194a6a4c642-1c50-56c5-e053-2a95a90ae3192021-02-19WarningsExact identifier
spl id: bbb3120e-d3f8-51e7-e053-2995a90a3194
spl set id: a6a4c642-1c50-56c5-e053-2a95a90ae319

Reported adverse events (FAERS/openFDA)#

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