Adventure Hand Sanitizer - Fragrance 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 - Fragrance 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]

front

Back

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1241663	ethanol 80 % Topical Spray	PSN	4
1241663	ethanol 0.8 ML/ML Topical Spray	SCD	4
1241663	ethanol 80 % Topical Spray	SY	4

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
77371-124-01	2024-06-19	C162847	48780-1	d6a99b39-3d01-a426-e053-dadaa90af4c2	Adventure Hand Sanitizer 80% Ethyl Alcohol Fragrance
77371-124-01	2024-01-30	C162847	48780-1	d6a99b39-3d01-a426-e053-dadaa90af4c2	Adventure Hand Sanitizer 80% Ethyl Alcohol Fragrance
77371-124-01	2022-07-20	C162847	48780-1	d6a99b39-3d01-a426-e053-dadaa90af4c2	Adventure Hand Sanitizer 80% Ethyl Alcohol Fragrance
77371-124-01	2022-01-28	C162847	48780-1	d6a99b39-3d01-a426-e053-dadaa90af4c2	Adventure Hand Sanitizer 80% Ethyl Alcohol Fragrance

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
77371-124-01	Adventure Hand Sanitizer - Fragrance 80%	38 mL in 1 BOTTLE, SPRAY	SPRAY	38		4

Products#

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

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

Adventure Hand Sanitizer - Fragrance 80%
Alcohol
WATER
ALOE VERA LEAF
PANTHENOL
HYDROXYETHYL CELLULOSE, UNSPECIFIED
PROPANEDIOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
77371-124	77371-124-01

Ingredients#

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

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

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
ALCOHOL	3K9958V90M	ACTIB
ALOE VERA LEAF	ZY81Z83H0X	IACT
PANTHENOL	WV9CM0O67Z	IACT
HYDROXYETHYL CELLULOSE, UNSPECIFIED	T4V6TWG28D	IACT
PROPANEDIOL	5965N8W85T	IACT

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Adventure Hand Sanitizer - Fragrance 80%	ALCOHOL	NICETY SOLUTIONS LLC	a507c20e-37d8-ea80-e053-2a95a90a41d4	2026-01-29	Warnings	Exact identifier ndc (package): 77371-124-01 ndc (product): 77371-124 ndc11 (package): 77371012401 spl id: 49903c54-83dc-1e0b-e063-6394a90aa4a7 spl set id: a507c20e-37d8-ea80-e053-2a95a90a41d4

Reported adverse events (FAERS/openFDA)#

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