SannyTize Hand Sanitizer Wipe

Manufacturer
Dynarex Corporation
Effective date
2024-11-20
Label type
HUMAN OTC DRUG LABEL
Version
10
Source
full-release
Hydrated at
2026-06-01 00:38:15

Label at a glance#

ProductSannyTize Hand Sanitizer Wipe
Active ingredientALCOHOL
Label structure9 sections

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient                         Purpose

Ethyl Alcohol 70%                   Antiseptic Wipe

WARNINGS

WARNINGS SECTION

  • For external use only
  • Flammable, keep away from fire and flame
  • When using this product avoid contact with eyes. In case of eye contact, rinse with water to remove.
  • Stop use and ask a doctor if irritation and redness develops

PURPOSE

OTC - PURPOSE SECTION

Antiseptic handwash

INDICATIONS & USAGE

INDICATIONS & USAGE SECTION

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

DOSAGE & ADMINISTRATION

DOSAGE & ADMINISTRATION SECTION

Wet hands thoroughly with product and allow to dry without wiping.

KEEP OUT OF REACH OF CHILDREN

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.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Inactive ingredients: Water, Glycerin, Propylene glycol, Diazolidinyl urea, Aloe barbadensis leaf juice, Polysorbate 20, Carbomer, Tocopherol acetate, Methylparaben, Propylparaben, Triethanolamine

RECENT MAJOR CHANGES SECTION

- Content of Labeling

- Indications and Usage Section

- Date Incorporated 09/2020

- Content of labeling

- Dosage and Administration Section

- Date incorporated 09/2020

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1306 IN Master1306 IN MasterDynarex SannyTizer HandSanitizing Wipes

Sannywipe.jpg

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1489307ethanol 70 % Medicated PadPSN10
1489307ethanol 0.7 ML/ML Medicated PadSCD10
1489307ethanol 70 % Medicated PadSY10
1489307ethanol 70 % Medicated WipesSY10
1489307ethyl alcohol 70 % ClothSY10

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
67777-320-01SannyTize Hand Sanitizer Wipe135 in 1 CANISTERGEL13510
67777-320-01SannyTize Hand Sanitizer Wipe3.42 mL in 1 PATCHGEL3.4210
67777-320-02SannyTize Hand Sanitizer Wipe1620 in 1 CASEGEL162010

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
67777-320SANNYTIZE HAND SANITIZER WIPE (ALCOHOL) GEL [DYNAREX CORPORATION]10Legacy NDC, 3 package rows20241122_25a1746f-9279-47a7-9224-3dfa2f2445c9.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
67777-320-01EA - Each67777-320be8fb8db-fd9d-41cf-b8bf-ca81294e618b12023-08-08
67777-320-02EA - Each67777-320fba47d4e-5263-4d44-a48e-8701639178f912023-08-08

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
67777-32067777-320-01, 67777-320-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 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
27593452-9103-0bb6-e063-6394a90af43625a1746f-9279-47a7-9224-3dfa2f2445c92024-11-20WarningsExact identifier
spl id: 27593452-9103-0bb6-e063-6394a90af436
spl set id: 25a1746f-9279-47a7-9224-3dfa2f2445c9

Reported adverse events (FAERS/openFDA)#

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