Fikes Northwest Non-Alcohol Foaming Instant Hand Sanitizer

Manufacturer
Fikes Northwest, Corp. | Canberra Corporation
Effective date
2010-01-08
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:23:13

Label at a glance#

ProductFikes Northwest Non-Alcohol Foaming Instant Hand Sanitizer
Active ingredientbenzalkonium chloride
Label structure6 sections

Indications and uses

For hand sanitizing to decrease bacteria on the skin Recommended for repeated use

Dosage and administration

Pump a small amount of foam into palm of hand Rub thoroughly over all surfaces of both hands Rub hands together briskly until dry Inactive Ingredients Water, dihydroxpropyl PEG-5 linoleammonium chloride, glycereth-2 cocoate, behentrimonium chloride, dihydroxyethyl cocamine oxide, fragrance

Label contents#

Full prescribing information#

Active Ingredient:

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.1%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

  • For hand sanitizing to decrease bacteria on the skin
  • Recommended for repeated use

Warning

WARNINGS SECTION

For external use only

OTC - WHEN USING SECTION

When using this product avoid contact with eyes. In case of eye contact, flush eyes with water. •

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or redness develops, or if condition persists for more than 72 hours. •

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Pump a small amount of foam into palm of hand
  • Rub thoroughly over all surfaces of both hands
  • Rub hands together briskly until dry

INACTIVE INGREDIENT SECTION

Inactive Ingredients Water, dihydroxpropyl PEG-5 linoleammonium chloride, glycereth-2 cocoate, behentrimonium chloride, dihydroxyethyl cocamine oxide, fragrance

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Fikes Northwest

Non AlcoholFoaming Instant Hand Sanitizer

• Enhanced with Moisturizers

• Kills disease causing germs within seconds

• Effective against MRSA, VRE, E. coli (0157:H7) Staphylococcus, Streptococcus and other organisms

• Assists with OSHA Bloodborne Pathogen Standard Compliance

See side panel for additional information.

For Hospital and Professional Use Only

Net Contents: One Gallon (128 Fl. Oz.) 3.78 liters

Package Label
Package Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1038799benzalkonium chloride 0.1 % Topical FoamPSN1
1038799benzalkonium chloride 1 MG/ML Topical FoamSCD1
1038799benzalkonium chloride 0.1 % Topical FoamSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
50036-514-052019-10-21C16284748780-1956f9ecf-da2b-621f-e053-dbdaa90a74adNon AlcoholFoaming Instant Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
50036-514-05Fikes Northwest Non-Alcohol Foaming Instant Hand Sanitizer3785 mL in 1 BOTTLESOLUTION37851

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50036-514FIKES NORTHWEST NON-ALCOHOL FOAMING INSTANT HAND SANITIZER (HUSKY 514) SOLUTION [FIKES NORTHWEST, CORP.]1Legacy NDC, 1 package rows20100113_648eda6b-d897-4ab2-93f5-ed6954326c7c.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
benzalkonium chlorideACTIVE INGREDIENTF5UM2KM3W71
benzalkoniumACTIVE MOIETY7N6JUD5X6Y1
behentrimonium chlorideINACTIVE INGREDIENTX7GNG3S47T1
dihydroxyethyl cocamine oxideINACTIVE INGREDIENT8AR51R3BL51
dihydroxypropyl peg-5 linoleammonium chlorideINACTIVE INGREDIENT0Y0NQR2GH11
glycereth-2 cocoateINACTIVE INGREDIENTJWM00VS7HC1
waterINACTIVE INGREDIENT059QF0KO0R1

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
50036-51450036-514-05

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Source Document#

Source XML · Source PDF

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
a1c2ade4-3511-4214-be58-9da4c5eb3108648eda6b-d897-4ab2-93f5-ed6954326c7c2010-01-08WarningsExact identifier
spl id: a1c2ade4-3511-4214-be58-9da4c5eb3108
spl set id: 648eda6b-d897-4ab2-93f5-ed6954326c7c

Reported adverse events (FAERS/openFDA)#

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