FDA.reportPublic FDA data

Steril Wize Antibacterial Foaming Hand Sanitizer

Manufacturer
Nostalgia Products LLC
Effective date
2020-07-07
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:20:28

Label at a glance#

ProductSteril Wize Antibacterial Foaming Hand Sanitizer
Active ingredientBENZALKONIUM CHLORIDE
Label structure7 sections

Dosage and administration

Pump a small amount of foam into palm of the hand. Rub thoroughly over all surfaces of both hands. Rub hands together briskly unit dry.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.1%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Use

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

For external use only.

When using this product

OTC - WHEN USING SECTION

If irritation or redness develops and conditions persist.

Stop use and ask a doctor

OTC - STOP USE SECTION

If irritation or redness develops and conditions persist.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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 the hand.
  • Rub thoroughly over all surfaces of both hands.
  • Rub hands together briskly unit dry.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Cetrimonium Chloride, Laurtrimonium Chloride, Dihydroxyethyl Cocamine Oxide, Glycereth-17 Cocoate, itric Acid.

OTC - QUESTIONS SECTION

In Case of Emergency Call Chemtrec 800-424-9300

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

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
77051-004-372022-01-28C16284748780-1d6a99b39-9097-a426-e053-dadaa90af4c2Steril-Wize Anti-Bacterial Foaming Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
77051-004-37Steril Wize Antibacterial Foaming Hand Sanitizer3785 mL in 1 BOTTLESOLUTION37851

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
77051-004STERIL WIZE ANTIBACTERIAL FOAMING HAND SANITIZER (BENZALKONIUM CHLORIDE) SOLUTION [NOSTALGIA PRODUCTS LLC]1Legacy NDC, 1 package rows20200708_a9dea7d0-ea83-8b93-e053-2995a90a345a.zip

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
77051-00477051-004-37

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
CETRIMONIUM CHLORIDEUC9PE95IBPIACT
LAURTRIMONIUM CHLORIDEA81MSI0FICIACT
DIHYDROXYETHYL COCAMINE OXIDE8AR51R3BL5IACT
GLYCERETH-17 COCOATE3057VPT0KCIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB

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
a9dea7d0-ea84-8b93-e053-2995a90a345aa9dea7d0-ea83-8b93-e053-2995a90a345a2020-07-07WarningsExact identifier
spl id: a9dea7d0-ea84-8b93-e053-2995a90a345a
spl set id: a9dea7d0-ea83-8b93-e053-2995a90a345a

Reported adverse events (FAERS/openFDA)#

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