FDA.reportPublic FDA data

SannyTize Hand Sanitizer

Manufacturer
Dynarex Corporation
Effective date
2024-01-24
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 00:07:55

Label at a glance#

ProductSannyTize Hand Sanitizer
Active ingredientALCOHOL
Label structure22 sections

Dosage and administration

Wet hands thoroughly with product and allow to dry without wiping

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70%

Purpose

OTC - PURPOSE SECTION

Antiseptic Handwash

Use

INDICATIONS & USAGE SECTION

  • For hand washing to decrease bacteria on the skin.

Warnings

WARNINGS SECTION

For External Use Only

Flammable. Keep away from fire or flame

Do not use

OTC - DO NOT USE SECTION

In the eyes.

When using this product

OTC - WHEN USING SECTION

• Avoid contact with eyes.

• In case of eye contact, rinse with water to remove

Stop use and ask a doctor if

OTC - STOP USE SECTION

Irritation and redness develop.

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 (1-800-222-1222) right away.

Directions

DOSAGE & ADMINISTRATION SECTION

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

Other Information

OTHER SAFETY INFORMATION

  • Do not store above 110°F (43ºC)
  • May discolor some fabrics
  • Recommended for repeated use

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Aloe Vera Leaf Extract, Carbopol Ultrez 10, Fragrance, Glycerin, Propylene Glycol, Purified Water,Triethanolamine

Questions?

OTC - QUESTIONS SECTION

1-888-396-2739 Monday - Friday, 9AM - 5PM EST

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1428-BX-GVIN0101428-BX-GVIN0101428 Hand Sanitizer

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1427 Hand Sanitizer

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1427-BX-GVIN0101427-BX-GVIN0101427 Hand Sanitizer

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1429-BX-GVIN0101429-BX-GVIN0101429 Hand Sanitizer

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1431- GVIN0101431- GVIN0101431 Hand Sanitizer

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1432-GVIN0101432-GVIN0101432 Hand Sanitizer

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1433-GVIN0101433-GVIN0101433 Hand Sanitizer

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1427-BX-MASTER1427-BX-MASTER1427 Hand Sanitizer

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1428-BX-MASTER1428-BX-MASTER1428 Hand Sanitizer

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1429-BX-MASTER1429-BX-MASTER1429 Hand Sanitizer

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1431-IN-MASTER1431-IN-MASTER1431 Hand Sabitizer

Labels

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1432-IN-MASTER1432-IN-MASTER1432 Hand Sanitizer

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1433-BX-MASTER1433-BX-MASTER1433 Hand Sanitizer

Label 1433UB-10

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1433UB-10_BX_MASTER1433UB-10_BX_MASTER1433UB-10

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN4
581662ethanol 0.7 ML/ML Topical GelSCD4
581662ethanol 70 % Topical GelSY4
581662ethyl alcohol 70 % Topical GelSY4

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
67777-010-01SannyTize Hand Sanitizer144 in 1 CASEGEL1444
67777-010-02SannyTize Hand Sanitizer144 in 1 CASEGEL1444
67777-010-03SannyTize Hand Sanitizer96 in 1 CASEGEL964
67777-010-04SannyTize Hand Sanitizer48 in 1 CASEGEL484
67777-010-05SannyTize Hand Sanitizer12 in 1 CASEGEL124
67777-010-06SannyTize Hand Sanitizer1728 in 1 CASEGEL17284
67777-010-10SannyTize Hand Sanitizer29.5 mL in 1 BOTTLEGEL29.54
67777-010-11SannyTize Hand Sanitizer24 in 1 BOXGEL244
67777-010-12SannyTize Hand Sanitizer59 mL in 1 BOTTLEGEL594
67777-010-13SannyTize Hand Sanitizer24 in 1 BOXGEL244
67777-010-14SannyTize Hand Sanitizer118.3 mL in 1 BOTTLEGEL118.34
67777-010-15SannyTize Hand Sanitizer24 in 1 BOXGEL244
67777-010-16SannyTize Hand Sanitizer236.5 mL in 1 BOTTLEGEL236.54
67777-010-17SannyTize Hand Sanitizer473 mL in 1 BOTTLE, PUMPGEL4734
67777-010-18SannyTize Hand Sanitizer144 in 1 BOXGEL1444
67777-010-18SannyTize Hand Sanitizer1.01 mL in 1 PACKETGEL1.014
67777-010-19SannyTize Hand Sanitizer10 in 1 BOXGEL104
67777-010-19SannyTize Hand Sanitizer1.01 mL in 1 PACKETGEL1.014
67777-010-20SannyTize Hand Sanitizer1000 in 1 CASEGEL10004

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
67777-010SANNYTIZE HAND SANITIZER (HAND SANITIZER) GEL [DYNAREX CORPORATION]4Current NDC, Legacy NDC, 19 package rows20240126_968713a5-64d3-86fc-e053-2995a90a088a.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
67777-01067777-010-10, 67777-010-11, 67777-010-01, 67777-010-12, 67777-010-13, 67777-010-02, 67777-010-14, 67777-010-15, 67777-010-03, 67777-010-16, 67777-010-04, 67777-010-17, 67777-010-05, 67777-010-18, 67777-010-06, 67777-010-19, 67777-010-20

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
ALOE VERA LEAFZY81Z83H0XIACT
GLYCERINPDC6A3C0OXIACT
TROLAMINE9O3K93S3TKIACT
WATER059QF0KO0RIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)59TL3WG5COIACT
ALCOHOL3K9958V90MACTIB

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
SannyTize Hand SanitizerHAND SANITIZERDynarex Corporation968713a5-64d3-86fc-e053-2995a90a088a2024-01-24WarningsExact identifier
ndc (package): 67777-010-15
ndc (package): 67777-010-02
ndc (package): 67777-010-20
ndc (package): 67777-010-12
ndc (package): 67777-010-18
ndc (package): 67777-010-19
ndc (package): 67777-010-03
ndc (package): 67777-010-17
ndc (package): 67777-010-14
ndc (package): 67777-010-13
ndc (package): 67777-010-11
ndc (package): 67777-010-10
ndc (package): 67777-010-05
ndc (package): 67777-010-04
ndc (package): 67777-010-16
ndc (package): 67777-010-01
ndc (package): 67777-010-06
ndc (product): 67777-010
ndc11 (package): 67777001012
ndc11 (package): 67777001002
ndc11 (package): 67777001006
ndc11 (package): 67777001013
ndc11 (package): 67777001005
ndc11 (package): 67777001014
ndc11 (package): 67777001001
ndc11 (package): 67777001019
ndc11 (package): 67777001004
ndc11 (package): 67777001010
ndc11 (package): 67777001017
ndc11 (package): 67777001015
ndc11 (package): 67777001011
ndc11 (package): 67777001018
ndc11 (package): 67777001016
ndc11 (package): 67777001020
ndc11 (package): 67777001003
spl id: 0fb7cb81-bb4b-f99f-e063-6294a90a336b
spl set id: 968713a5-64d3-86fc-e053-2995a90a088a

Reported adverse events (FAERS/openFDA)#

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