Germ Free Zone Sanitizing Wipe

Manufacturer: Germ Guards Incorporated
Effective date: 2017-06-01
Label type: HUMAN OTC DRUG LABEL
Version: 40
Source: full-release
Hydrated at: 2026-05-31 22:50:00

Label at a glance#

ProductGerm Free Zone Sanitizing Wipe

Active ingredientALCOHOL

Label structure8 sections

Indications and uses

Helps reduce becteria, fungl, and some viruses.

Dosage and administration

Tear open packet, wipe, discard.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

DRUG FACTS

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% (v/v)

Purpose

OTC - PURPOSE SECTION

Antimicrobia

Uses:

INDICATIONS & USAGE SECTION

Helps reduce becteria, fungl, and some viruses.

WARNINGS SECTION

For external use only.

OTC - DO NOT USE SECTION

Flammable, keep away from heat and flame.
Do not use in or near eyes. If eye contact occurs flush thoroughly with water and seek medical care.
Avoid contact with broken skin.
Stop use and seek medical attention if irritation and redness occurs.
Ingestion may cause alcohol poisoning, if ingested contact a physician or local poison control center.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of accidental ingestion, seekprofessional assistance or contact a Poison Control Center immediately.

Directions:

DOSAGE & ADMINISTRATION SECTION

Tear open packet, wipe, discard.

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

purified water, Glycerol

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Principal Display Panel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1489307	ethanol 70 % Medicated Pad	PSN	40
1489307	ethanol 0.7 ML/ML Medicated Pad	SCD	40
1489307	ethanol 70 % Medicated Pad	SY	40
1489307	ethanol 70 % Medicated Wipes	SY	40
1489307	ethyl alcohol 70 % Cloth	SY	40

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
3c386306-c48a-413e-bb69-70cb268496f3	Product name	1	20210727
7792dadb-52b6-46b6-8fdf-80b1171065b5	Product name	1	20180810

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
71089-001-01	2020-01-31	C162847	48780-1	9d75b9d0-82a8-f424-e053-dadaa90a57ce	065bef41-0714-4c0b-949d-10b05992d727

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
71089-001-01	Germ Free Zone Sanitizing Wipe	3.0 mL in 1 PACKAGE	CLOTH	3.0		40
71089-001-01	Germ Free Zone Sanitizing Wipe	1 in 1 PACKAGE	CLOTH	1		40

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
71089-001	GERM FREE ZONE SANITIZING WIPE (ALCOHOL) CLOTH [GERM GUARDS INCORPORATED]	40	Legacy NDC, 2 package rows	20170601_065bef41-0714-4c0b-949d-10b05992d727.zip

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

Germ Free Zone Sanitizing Wipe
Alcohol
GLYCERIN
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
71089-001	71089-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ALCOHOL	3K9958V90M	ACTIB
GLYCERIN	PDC6A3C0OX	IACT
WATER	059QF0KO0R	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
f261e8cb-b6e7-49a0-b102-54063c85b59d			065bef41-0714-4c0b-949d-10b05992d727	2017-06-01	Warnings	Exact identifier spl id: f261e8cb-b6e7-49a0-b102-54063c85b59d spl set id: 065bef41-0714-4c0b-949d-10b05992d727

Reported adverse events (FAERS/openFDA)#

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