Hand Sanitizer

Manufacturer: Zink Holdings LLC
Effective date: 2020-08-24
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:25:39

Label at a glance#

ProductHand Sanitizer

Active ingredientALCOHOL

Label structure12 sections

Indications and uses

■ Hand sanitizer to help reduce bacteria on the skin. For use when soap and water are not available

Dosage and administration

■ Place enough product on hands to cover all surfaces. ■ Rub thoroughly into hands for at least 30 seconds. Allow to dry.

Storage and handling

■ Store between 15º-30ºC (59º-89ºF) ■ Avoid freezing and excessive heat above 40ºC (104ºF) ■ May discolor fabrics or surfaces.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 66%v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

■ Hand sanitizer to help reduce bacteria on the skin. 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 use

OTC - DO NOT USE SECTION

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

When using this product

OTC - WHEN USING SECTION

keep out of eyes, ears, ears and mouth. In case of eye contact immediately flush eyes thoroughly with water.

Stop use and ask a doctor

OTC - STOP USE SECTION

if irritation or rash occurs. These may be the signs of a serious condition.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of accidentail ingestion, contact a doctor or Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

■ Place enough product on hands to cover all surfaces. ■ Rub thoroughly into hands for at least 30 seconds. Allow to dry.

Other information

STORAGE AND HANDLING SECTION

■ Store between 15º-30ºC (59º-89ºF) ■ Avoid freezing and excessive heat above 40ºC (104ºF) ■ May discolor fabrics or surfaces.

Inactive ingredients

INACTIVE INGREDIENT SECTION

2-(perfluorohexyl)ethanol, PEG-10 acrylate/perfluorohexylethyl acrylate copolymer, purified water

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

package label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
2388174	ethanol 66 % Topical Foam	PSN	1
2388174	ethanol 0.66 ML/ML Topical Foam	SCD	1
2388174	ethanol 66 % Topical Foam	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
79332-002-28	2022-07-29	C162847	48780-1	e4f33bdf-a74b-d8a0-e053-dadaa90a6e4e	Zink Brntag Rhinestone Foam Sanitizer Alc66

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
79332-002-28	Hand Sanitizer	3790 mL in 1 BOTTLE, PLASTIC	LIQUID	3790		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
79332-002	HAND SANITIZER (ALCOHOL) LIQUID [ZINK HOLDINGS LLC]	1	Legacy NDC, 1 package rows	20200825_ad671fbe-bdce-b556-e053-2995a90acbfb.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

Hand Sanitizer
ALCOHOL
WATER
PEG-10 ACRYLATE/PERFLUOROHEXYLETHYL ACRYLATE COPOLYMER
2-(PERFLUOROHEXYL)ETHANOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
79332-002	79332-002-28

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
PEG-10 ACRYLATE/PERFLUOROHEXYLETHYL ACRYLATE COPOLYMER	D76Z87928N	IACT
2-(PERFLUOROHEXYL)ETHANOL	G2R5YO5N3V	IACT
ALCOHOL	3K9958V90M	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
ad672786-7ddb-b6da-e053-2995a90aed5e			ad671fbe-bdce-b556-e053-2995a90acbfb	2020-08-24	Warnings	Exact identifier spl id: ad672786-7ddb-b6da-e053-2995a90aed5e spl set id: ad671fbe-bdce-b556-e053-2995a90acbfb

Reported adverse events (FAERS/openFDA)#

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