Germ-Away

Manufacturer
Unico International Trading Corp | Dan Mor
Effective date
2026-01-08
Label type
HUMAN OTC DRUG LABEL
Version
8
Source
full-release
Hydrated at
2026-06-01 01:32:08

Label at a glance#

ProductGerm-Away
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Dosage and administration

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

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium chloride 0.1%

Purpose

OTC - PURPOSE SECTION

Anti-bacterial

Keep our 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.

Directions

INDICATIONS & USAGE SECTION

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

Fragrance

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, Fragranc

Directions

DOSAGE & ADMINISTRATION SECTION

Locate tear-notch on top of refill pouch. Tear straight across to open. Pull first wipe from center of roll through the pouch center opening. Thread wipe through dispenser nozzle. Use only upward pull dispensers (floor stand or wall units) so liquid does not drip out of pouch.

label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Germ-Away 1200Germ-Away 1200

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1038558benzalkonium chloride 0.13 % Medicated PadPSN8
1038558benzalkonium chloride 1.3 MG/ML Medicated PadSCD8
1038558benzalkonium chloride 0.13 % Topical ClothSY8
1038558benzalkonium chloride 0.13 % Topical SwabSY8
1038558benzalkonium chloride 0.13 GM per 100 GM Topical PadSY8
1038558benzalkonium chloride 0.13 GM per 100 GM Topical SwabSY8
1038558benzalkonium chloride 1 ML per 750 ML Topical SwabSY8

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130655315719286GTIN-13: 0655315719286
EAN-13: 0655315719286
GTIN-12: 655315719286
UPC-A: 655315719286
GTIN storage (14 digits): 00655315719286
a_006.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
74680-102-882022-06-02C16284748780-1d6a99b39-e14d-a426-e053-dadaa90af4c2Germ-Away
74680-102-882022-01-28C16284748780-1d6a99b39-e14d-a426-e053-dadaa90af4c2Germ-Away

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74680-102-88Germ-Away1200 g in 1 PACKAGECLOTH12008

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
74680-10274680-102-88

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-MICROBIALUnico International Trading Corpa7d35899-8b70-14f0-e053-2995a90a5ce82026-01-08WarningsExact identifier
ndc (package): 74680-102-88
ndc (product): 74680-102
ndc11 (package): 74680010288
spl id: 47e1ac82-62a9-a090-e063-6294a90a8a9e
spl set id: a7d35899-8b70-14f0-e053-2995a90a5ce8

Reported adverse events (FAERS/openFDA)#

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