Amora Spray Hand Sanitizer Watermelon

Manufacturer: I World LLC
Effective date: 2026-05-11
Label type: HUMAN OTC DRUG LABEL
Version: 4
Source: full-release
Hydrated at: 2026-06-01 01:57:40

Label at a glance#

ProductAmora Hand Sanitizer Watermelon

Active ingredientALCOHOL

Label structure8 sections

Indications and uses

For hand-washing to decrease bacteria on the skin.

Dosage and administration

Spray hands with product and allow to dry without wiping. For children under 6, use only under adult supervision. Not recommended for infants.

Contacts and useful links#

PhoneLabel contact1-212-244-5170

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% v/v

Purpose

OTC - PURPOSE SECTION

Antibacterial

Uses

INDICATIONS & USAGE SECTION

For hand-washing to decrease bacteria on the skin.

Warnings

WARNINGS SECTION

For external use only.

Flammabel, keep away from fire and flames

when using this product

OTC - WHEN USING SECTION

test on a small area of skin before full use.
keep out of eyes. In case of contact with eyes, flush throughly with water.
Avoid contact with broken skin.
Do not inhale or ingest.

Stop use and ask doctor if

OTC - STOP USE SECTION

allergy, 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

If product is swallowed, get medical help or contact a poison control centre right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Spray hands with product and allow to dry without wiping.
For children under 6, use only under adult supervision.
Not recommended for infants.

Other information

SPL UNCLASSIFIED SECTION

Do not store above 105° F
May discolor some fabrics
Harmful to wood finishes and plastics

Inactive ingredients

INACTIVE INGREDIENT SECTION

WATER (AQUA), FRAGRANCE (PARFUM), GLYCERIN, CITRULLUS LANATUS (WATERMELON) FRUIT EXTRACT, BUTYLENE GLYCOL, 1-2-HEXANEDIOL, HYDROXYACETOPHENONE.

Questions or comments?

OTC - QUESTIONS SECTION

1-212-244-5170 info@amora.beauty

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label3

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1041849	ethanol 70 % Topical Spray	PSN	4
1041849	ethanol 0.7 ML/ML Topical Spray	SCD	4
1041849	ethanol 70 % Topical Spray	SY	4

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
85179-039-00	Amora Hand Sanitizer Watermelon	45 mL in 1 BOTTLE	SPRAY	45		4

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

Amora Hand Sanitizer Watermelon
ALCOHOL
1,2-HEXANEDIOL
WATER
GLYCERIN
WATERMELON
BUTYLENE GLYCOL
HYDROXYACETOPHENONE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
85179-039	85179-039-00

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
1,2-HEXANEDIOL	TR046Y3K1G	IACT
WATER	059QF0KO0R	IACT
GLYCERIN	PDC6A3C0OX	IACT
WATERMELON	231473QB6R	IACT
BUTYLENE GLYCOL	3XUS85K0RA	IACT
HYDROXYACETOPHENONE	G1L3HT4CMH	IACT
ALCOHOL	3K9958V90M	ACTIB

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
Version	Effective date	Source	Hydrated
3	2026-05-08	weekly-update	2026-06-03 18:02:41
2	2026-02-10	monthly-update	2026-06-03 17:56:25

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
Amora Hand Sanitizer Watermelon	ALCOHOL	I World LLC	45f9b0a2-972f-4d44-aad1-8999313d4191	2026-05-11	Warnings	Exact identifier ndc (package): 85179-039-00 ndc (product): 85179-039 ndc11 (package): 85179003900 spl id: 518ee0af-e6b9-45c6-e063-6294a90a05ff spl set id: 45f9b0a2-972f-4d44-aad1-8999313d4191

Reported adverse events (FAERS/openFDA)#

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