Adventure Hand Sanitizer - Unscented 80%

Manufacturer
NICETY SOLUTIONS LLC
Effective date
2026-01-29
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 01:35:59

Label at a glance#

ProductAdventure Hand Sanitizer - Unscented 80%
Active ingredientALCOHOL
Label structure7 sections

Dosage and administration

Spray hands thoroughly. Rub hands together until dry.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 80% v/v

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Use

INDICATIONS & USAGE SECTION

For hand sanitizing to decrease bacteria on skin.

Warnings

WARNINGS SECTION

For external use only

Flammable, keep away from fire and flame

Do not use

OTC - DO NOT USE SECTION

in the eyes

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact an Poison Control Center right away.

Stop use and ask a doctor if

OTC - STOP USE SECTION

redness or irritation develops and persists for more than 72 hours

Directions

DOSAGE & ADMINISTRATION SECTION

Spray hands thoroughly. Rub hands together until dry.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Propanediol, Aloe Vera Powder, Panthenol, Hydroxyethylcellulose

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Adventure Hand Santitizer

By the makers of Shower Pouch

Remove odors

Kills germs on the go

1.3 fl oz [38 ml]

frontfront

backback

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1241663ethanol 80 % Topical SprayPSN4
1241663ethanol 0.8 ML/ML Topical SpraySCD4
1241663ethanol 80 % Topical SpraySY4

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130753936732339GTIN-13: 0753936732339
EAN-13: 0753936732339
GTIN-12: 753936732339
UPC-A: 753936732339
GTIN storage (14 digits): 00753936732339
Label 6 Back Unscented_Sanitizer_Ethyl_80_Final_No_Artifact.jpg

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
77371-023-01Adventure Hand Sanitizer - Unscented 80%38 mL in 1 BOTTLE, SPRAYSPRAY384

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
77371-02377371-023-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Source Document#

Source XML · Source PDF

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
Adventure Hand Sanitizer - Unscented 80%ALCOHOLNICETY SOLUTIONS LLCa5077eb2-4adb-0680-e053-2995a90a2cef2026-01-29WarningsExact identifier
ndc (package): 77371-023-01
ndc (product): 77371-023
ndc11 (package): 77371002301
spl id: 49903f8e-a791-45c3-e063-6294a90a14e6
spl set id: a5077eb2-4adb-0680-e053-2995a90a2cef

Reported adverse events (FAERS/openFDA)#

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