Sea and Ski Advanced 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 Advanced Hand Sanitizer

Active ingredientALCOHOL

Label structure8 sections

Label contents#

Full prescribing information#

DOSAGE & ADMINISTRATION SECTION

dosage

WARNINGS SECTION

warnings

INDICATIONS & USAGE SECTION

indications and usage

INACTIVE INGREDIENT SECTION

Inactive drug

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

OTC - PURPOSE SECTION

purpose

OTC - ACTIVE INGREDIENT SECTION

active ingredient

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Sea&Ski Advanced Hand Sanitizer

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
73440-2131-1	2023-01-30	C162847	48780-1	f386c64a-3b13-0266-e053-dadaa90a7c1a	Sea&Ski Advanced Hand Sanitizer 64oz

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
73440-2131-1	Sea and Ski Advanced Hand Sanitizer	1814.37 g in 1 BOTTLE, PUMP	GEL	1814.37		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
73440-2131	SEA AND SKI ADVANCED HAND SANITIZER (ETHYL ALCOHOL) GEL [CROSS-BRANDS CONTRACT FILLING]	2	Legacy NDC, 1 package rows	20210220_a0fdd16c-fdcf-73b3-e053-2995a90a4ae5.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 Advanced Hand Sanitizer
Ethyl Alcohol
ALCOHOL
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
73440-2131	73440-2131-1

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
bbb395d2-5b93-632a-e053-2a95a90a928d			a0fdd16c-fdcf-73b3-e053-2995a90a4ae5	2021-02-19	Warnings	Exact identifier spl id: bbb395d2-5b93-632a-e053-2a95a90a928d spl set id: a0fdd16c-fdcf-73b3-e053-2995a90a4ae5

Reported adverse events (FAERS/openFDA)#

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