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: 2
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

Uses to decrease bacteria on the skin that could cause diesease 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 Ingredients

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient section

Alcohol 62%

Purpose

OTC - PURPOSE SECTION

Purpose Section

Antiseptic

Uses

INDICATIONS & USAGE SECTION

Uses Section

Uses to decrease bacteria on the skin that could cause diesease

recommended for repeated use

Warnings

WARNINGS SECTION

Warnings Section

For external use only: Hands

Flammable, keep away from fire or flame

When using

OTC - DO NOT USE SECTION

When using Section

When 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 use section

Stop 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 children section

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

Directions

DOSAGE & ADMINISTRATION SECTION

Directions section

wet 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 information section

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

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Inactive ingredients section

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

*contains one or more of these ingredients

Package Label Princial Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Front Label

Sea & Ski Ultra Light Dri-Gel Hand Sanitizer Moisturizing Aloe Alcohol Antispetic Helps Reduce Bacteria 2.4FL OZ (71 mL)

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
581660	ethanol 62 % Topical Gel	PSN	2
581660	ethanol 0.62 ML/ML Topical Gel	SCD	2
581660	ethanol 62 % Topical Gel	SY	2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
73440-2135-1	2023-01-30	C162847	48780-1	f386c64a-02d8-0266-e053-dadaa90a7c1a	Sea & Ski Advanced Hand Sanitizer 2.4oz

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
73440-2135-1	Sea and Ski Advance Hand Sanitizer	237 mL in 1 BOTTLE	GEL	237		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
73440-2135	SEA AND SKI ADVANCE HAND SANITIZER (ETHYL ALCOHOL) GEL [CROSS-BRANDS CONTRACT FILLING]	2	Legacy NDC, 1 package rows	20210220_aecd94eb-50f9-2191-e053-2a95a90a1991.zip

Products#

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

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

Sea and Ski Advance Hand Sanitizer
Ethyl Alcohol
ALCOHOL
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
73440-2135	73440-2135-1

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
Name	UNII	Kind
ALCOHOL	3K9958V90M	ACTIB
WATER	059QF0KO0R	IACT

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
bbb3029f-0577-a396-e053-2a95a90a071d			aecd94eb-50f9-2191-e053-2a95a90a1991	2021-02-19	Warnings	Exact identifier spl id: bbb3029f-0577-a396-e053-2a95a90a071d spl set id: aecd94eb-50f9-2191-e053-2a95a90a1991

Reported adverse events (FAERS/openFDA)#

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