Germ Away

Manufacturer
Unico International Trading Corp | Dan Mor
Effective date
2026-01-08
Label type
HUMAN OTC DRUG LABEL
Version
10
Source
full-release
Hydrated at
2026-06-01 01:32:08

Label at a glance#

ProductGerm Away
Active ingredientBENZALKONIUM CHLORIDE
Label structure9 sections

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.1%

Keep out of the reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children, except with adult supervision.

Warnings

WARNINGS SECTION

For external use only. Do not use in the eyes.

Keep out of eyes. In case of eye contact, rinse with water. If irritation develops, discontinue use. Consult doctor if irritation persists for more than 72 hours.

If swallowed, seek medical attention or contact a Poison Control Center.

Use

DOSAGE & ADMINISTRATION SECTION

For use: gently pull wipe from the dispenser feed at an angle and in a downward motion. wet hands or surface thoroughly with the product and let dry, discard wipe in trash

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Aqua, Decyl Glucoside, Glycerin, Sodium Hydroxymethylglycinate, Citric Acid, PEG-12 Dimethicone Copolyol, Tetrasodium EDTA, Potassium Sorbate, Sodium Benzoate, Aloe Barbadensis Leaf Extract, Chamomilla Recutita (Matricaria) Flower Extract, Allantoin, Panthenol, Tocopheryl Acetate

Purpose

OTC - PURPOSE SECTION

Anti-bacterial

To dispense

DOSAGE & ADMINISTRATION SECTION

Break tab on bucket rim and pull off cover. Open bag inside to expose wipes. Then thread center wipe through the lid. Replace bucket cover to maintain moisture.

To use

INDICATIONS & USAGE SECTION

Pull one sheet from pack. Sanitize hands or other affected area. Discard in trash after use. Do not flush. Close tab after use to retain moisture.

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Germ Away 400Germ Away 400

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1038558benzalkonium chloride 0.13 % Medicated PadPSN10
1038558benzalkonium chloride 1.3 MG/ML Medicated PadSCD10
1038558benzalkonium chloride 0.13 % Topical ClothSY10
1038558benzalkonium chloride 0.13 % Topical SwabSY10
1038558benzalkonium chloride 0.13 GM per 100 GM Topical PadSY10
1038558benzalkonium chloride 0.13 GM per 100 GM Topical SwabSY10
1038558benzalkonium chloride 1 ML per 750 ML Topical SwabSY10

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130655315719576GTIN-13: 0655315719576
EAN-13: 0655315719576
GTIN-12: 655315719576
UPC-A: 655315719576
GTIN storage (14 digits): 00655315719576
a_004.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
74680-101-632022-06-02C16284748780-1d6a99b39-aef3-a426-e053-dadaa90af4c2Germ Away
74680-101-632022-01-28C16284748780-1d6a99b39-aef3-a426-e053-dadaa90af4c2Germ Away

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74680-101-63Germ Away400 g in 1 CONTAINERCLOTH40010

Products#

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

DailyMed product names page 1 of 1 · 25 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74680-10174680-101-63

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 22 matching rows.

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Germ AwayANTI-MICROBIAL WIPEUnico International Trading Corpa6b4eec4-0b12-3a00-e053-2a95a90a78352026-01-08WarningsExact identifier
ndc (package): 74680-101-63
ndc (product): 74680-101
ndc11 (package): 74680010163
spl id: 47e1b36f-c28c-bf41-e063-6394a90a32e1
spl set id: a6b4eec4-0b12-3a00-e053-2a95a90a7835

Reported adverse events (FAERS/openFDA)#

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