Hand Sanitizer

Manufacturer: COTTON ON USA INC. | Nantong Health & Beyond Hygienic Products Inc.
Effective date: 2020-10-06
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:31:16

Label at a glance#

ProductHand Sanitizer

Active ingredientALCOHOL

Label structure12 sections

Indications and uses

Hand Sanitizer to help reduce bacteria that potentially can cause disease.

Dosage and administration

Spray on hands and rub together until dry. Supervise children in the use of this product.

Storage and handling

Store at 30C (86F) Keep out of direct sunlight

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 66%...Purpose: Antimicrobial

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

Hand Sanitizer to help reduce bacteria that potentially can cause disease.

Warnings

WARNINGS SECTION

Flammable. For external use only. Keep away from heat or flame

Do not use

OTC - DO NOT USE SECTION

When using this product do not use in or around the eyes. If contact occurs, rinse eyes thoroughly with water. Do not use on broken or irritated skin.

OTC - WHEN USING SECTION

When using this product do not use in or around the eyes. If contact occurs, rinse eyes thoroughly with water. Do not use on broken or irritated skin.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash occurs.

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.

Other information

STORAGE AND HANDLING SECTION

Store at 30C (86F)
Keep out of direct sunlight

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water (aqua), Glycerin, Propylene Glycol, Aloe Barbadensis Leaf Juice, Fragrance

Directions

DOSAGE & ADMINISTRATION SECTION

Spray on hands and rub together until dry.
Supervise children in the use of this product.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

17.5 mL

Strawberry Scented

Alchol 66%

Label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
90015-005-01	2024-01-30	C162847	48780-1	1030e365-5d21-111a-e063-dadaa90a10e2	FOUNDATION 2020 Q2 HAND SANITIZER ALCOHOL USA 66 Strawberry - Pink

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
90015-005-01	Hand Sanitizer	17.5 mL in 1 BOTTLE, SPRAY	SPRAY	17.5		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
90015-005	HAND SANITIZER (ALCOHOL) SPRAY [COTTON ON USA INC.]	1	Legacy NDC, 1 package rows	20201009_b1033814-2644-568b-e053-2a95a90adde0.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

Hand Sanitizer
ALCOHOL
GLYCERIN
PROPYLENE GLYCOL
WATER
ALOE VERA LEAF

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
90015-005	90015-005-01

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
GLYCERIN	PDC6A3C0OX	IACT
PROPYLENE GLYCOL	6DC9Q167V3	IACT
WATER	059QF0KO0R	IACT
ALCOHOL	3K9958V90M	ACTIB
ALOE VERA LEAF	ZY81Z83H0X	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
b10337dd-83cc-ba02-e053-2a95a90aabfd			b1033814-2644-568b-e053-2a95a90adde0	2020-10-06	Warnings	Exact identifier spl id: b10337dd-83cc-ba02-e053-2a95a90aabfd spl set id: b1033814-2644-568b-e053-2a95a90adde0

Reported adverse events (FAERS/openFDA)#

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