Hand Sanitizer

Manufacturer: POWELL INDUSTRIES INC
Effective date: 2020-09-02
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:26:40

Label at a glance#

ProductHand Sanitizer

Active ingredientISOPROPYL ALCOHOL

Label structure12 sections

Dosage and administration

wipe asneeded

Storage and handling

Store between 15-30C (59-86F) Avoid freezing and excessive heat above 40C (104F)

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Isopropyl Alcohol 70% v/v. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer

Use

INDICATIONS & USAGE SECTION

Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings

WARNINGS SECTION

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

DO NOT FLUSH

Do not use

OTC - DO NOT USE SECTION

in children less than 2 months of age
on open skin wounds

OTC - WHEN USING SECTION

When using this product use with adequate ventilation. In case of contact with eyes, rinse eyes thoroughly with water for 15 minutes.

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

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.

Directions

DOSAGE & ADMINISTRATION SECTION

wipe asneeded

Other information

STORAGE AND HANDLING SECTION

Store between 15-30C (59-86F)
Avoid freezing and excessive heat above 40C (104F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

deionized water

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

WIPES226 ml NDC: 80210-001-01

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
797544	isopropyl alcohol 70 % Medicated Pad	PSN	1
797544	isopropyl alcohol 0.7 ML/ML Medicated Pad	SCD	1
797544	isopropyl alcohol 70 % Medicated Pad	SY	1
797544	isopropyl alcohol 70 % Topical Cloth	SY	1
797544	isopropyl alcohol 70 % Topical Swab	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
80210-001-01	2021-07-23	C162847	48780-1	c7ccaba7-201c-fd44-e053-dadaa90aa01b	hand sanitizing wipes

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
80210-001-01	Hand Sanitizer	226 mL in 1 BAG	CLOTH	226		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
80210-001	HAND SANITIZER (ISOPROPYL ALCOHOL) CLOTH [POWELL INDUSTRIES INC]	1	Legacy NDC, 1 package rows	20200903_ae571e70-cfbb-c937-e053-2995a90aceb7.zip

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

Hand Sanitizer
Isopropyl Alcohol
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
80210-001	80210-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
ISOPROPYL ALCOHOL	ND2M416302	ACTIB

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
ae56f2e1-288c-3104-e053-2995a90aae3f			ae571e70-cfbb-c937-e053-2995a90aceb7	2020-09-02	Warnings	Exact identifier spl id: ae56f2e1-288c-3104-e053-2995a90aae3f spl set id: ae571e70-cfbb-c937-e053-2995a90aceb7

Reported adverse events (FAERS/openFDA)#

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