Hand Sanitizer

Manufacturer: Raining Rose, Inc.
Effective date: 2025-04-07
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-06-01 00:58:44

Label at a glance#

ProductHand Sanitizer

Active ingredientALCOHOL

Label structure10 sections

Storage and handling

Do not store above 105 F May discolor some fabrics.

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients
Alcohol 62%

OTC - PURPOSE SECTION

Purpose
Antiseptic

WARNINGS SECTION

Warnings

Flammable, keep away from open flame and sources of heat. For external use only. Do not ingest.

Do not use in eyes. In case of eye contact flush thoroughly with water and seek medical attention.

OTC - STOP USE SECTION

Stop use and ask doctor if irritation and redness develops and persists for more than 72 hours. Do not use if you are allergic to any ingredients.

OTC - 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.

DOSAGE & ADMINISTRATION SECTION

Directions

Use 1.5mL and rub thoroughly into hands for at least 30 seconds. Allow to dry.
Does not require rinsing.

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Aloe Barbadenis Leaf Juice, Glycerin, Propylene Glycol, Vanilla Fragrance, Water.

INDICATIONS & USAGE SECTION

Use

Kills some harmful bacteria/germs.
For occasional use, as needed.

Other Information

STORAGE AND HANDLING SECTION

Do not store above 105 F
May discolor some fabrics.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image of bottle label

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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
65692-1003-1	Hand Sanitizer	17 mL in 1 BOTTLE	GEL	17		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
65692-1003	HAND SANITIZER (ETHYL ALCOHOL) GEL [RAINING ROSE, INC.]	2	Current NDC, Legacy NDC, 1 package rows	20250409_43ab2651-6e0a-3d48-e054-00144ff88e88.zip

Products#

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

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

Hand Sanitizer
ETHYL ALCOHOL
ALCOHOL
WATER
ALOE VERA LEAF
GLYCERIN
PROPYLENE GLYCOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
65692-1003	65692-1003-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ALCOHOL	3K9958V90M	ACTIB
WATER	059QF0KO0R	IACT
ALOE VERA LEAF	ZY81Z83H0X	IACT
GLYCERIN	PDC6A3C0OX	IACT
PROPYLENE GLYCOL	6DC9Q167V3	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
Hand Sanitizer	ETHYL ALCOHOL	Raining Rose, Inc.	43ab2651-6e0a-3d48-e054-00144ff88e88	2025-04-07	Warnings	Exact identifier ndc (package): 65692-1003-1 ndc (product): 65692-1003 ndc11 (package): 65692100301 spl id: 323a681c-2a07-12a3-e063-6394a90aca02 spl set id: 43ab2651-6e0a-3d48-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

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