FDA.reportPublic FDA data

Germ-Away

Manufacturer
Unico International Trading Corp | Dan Mor
Effective date
2020-08-22
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:25:31

Label at a glance#

ProductGerm-Away
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Dosage and administration

Pull one sheet from packet.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium chloride 01%

Purpose

OTC - PURPOSE SECTION

Anti-bacterial

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.

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, Fragrance

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 packet.

Use

DOSAGE & ADMINISTRATION SECTION

Sanitize hands or other affected area. Discard in trash after use. Do not flush. Reseal packet after use to retain moisture.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Germ-AwayGerm-Away

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
74680-106-172022-01-28C16284748780-1d6a99b39-face-a426-e053-dadaa90af4c2Germ-Away

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74680-106-17Germ-Away50 in 1 JARCLOTH502

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74680-106GERM-AWAY (ANTI-MICROBIAL) CLOTH [UNICO INTERNATIONAL TRADING CORP]2Legacy NDC, 1 package rows20200823_a7d58639-34cd-51fa-e053-2995a90a6a72.zip

Products#

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

DailyMed product names page 1 of 1 · 28 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74680-10674680-106-17

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 25 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
SANDALORE1XL3NL51UUIACT
EDETATE SODIUMMP1J8420LUIACT
PEG-12 DIMETHICONE (300 CST)ZEL54N6W95IACT
SODIUM HYDROXYMETHYLGLYCINATEDIG6BWZ9XTIACT
POTASSIUM SORBATE1VPU26JZZ4IACT
4-TERT-BUTYLCYCLOHEXYL ACETATE21EUM2B8UCIACT
ANHYDROUS CITRIC ACIDXF417D3PSLIACT
PANTHENOLWV9CM0O67ZIACT
2-ISOBUTYL-4-METHYLTETRAHYDROPYRAN-4-OLVK5ZHH2T3FIACT
TETRAHYDROLINALOOLUM4XS5M134IACT
2,2'-OXYDIPROPANOL7KOI7K0DHIIACT
ALLANTOIN344S277G0ZIACT
GLYCERINPDC6A3C0OXIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
CHAMOMILEFGL3685T2XIACT
DECYL GLUCOSIDEZ17H97EA6YIACT
SODIUM BENZOATEOJ245FE5EUIACT
ALOE VERA LEAFZY81Z83H0XIACT
EUCALYPTOLRV6J6604TKIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
3,7-DIMETHYL-1-OCTANOLDPY9K1927CIACT
COUMARINA4VZ22K1WTIACT
DIPHENYL ETHER3O695R5M1UIACT
CP FORMATECEB8Q6WHK2IACT

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
ad7b9e5a-cdf9-48db-e053-2a95a90aca8aa7d58639-34cd-51fa-e053-2995a90a6a722020-08-22WarningsExact identifier
spl id: ad7b9e5a-cdf9-48db-e053-2a95a90aca8a
spl set id: a7d58639-34cd-51fa-e053-2995a90a6a72

Reported adverse events (FAERS/openFDA)#

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