Ultra Defense Advanced Hand Sanitizer

Manufacturer
Republic Nail, S.A. de C.V.
Effective date
2020-06-01
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:15:51

Label at a glance#

ProductUltra Defense Advanced Hand Sanitizer
Active ingredientALCOHOL
Label structure8 sections

Indications and uses

hand sanitizer to help decrease baceteria on the skin  when water, soap & towel are not available recommended for repetaed use

Dosage and administration

pump as needed into your palms and thoroughly spread on both hands. rub into skin until dry.

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

  • hand sanitizer to help decrease baceteria on the skin 
  • when water, soap & towel are not available
  • recommended for repetaed use

Warnings

WARNINGS SECTION

For external use only.

Flammable, Keep away from fire or flame.

Do not apply around eyes.

Do not use

OTC - DO NOT USE SECTION

in ears & mouth

When using this product,

OTC - WHEN USING SECTION

avoid contact with eyes. In case of contact flush eyes with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

redness or irritation develop and persist for more than 72 hours.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Children must be supervised in use of this product.

Directions

DOSAGE & ADMINISTRATION SECTION

  • pump as needed into your palms and thoroughly spread on both hands.
  • rub into skin until dry.

Other informaton

SPL UNCLASSIFIED SECTION

  • store at 20° C (68° to 77° F)
  • may discolor fabrics.

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, glycerin, carbomer, Treithanolamine.

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

Packaging 250mL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

250mL250mL

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1305100ethanol 75 % Topical GelPSN2
1305100ethanol 0.75 ML/ML Topical GelSCD2
1305100ethanol 75 % Topical GelSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
77618-001-012021-07-23C16284748780-1c7ccaba7-228c-fd44-e053-dadaa90aa01bUltra Defense Advanced Hand Sanitizer
77618-001-022021-07-23C16284748780-1c7ccaba7-228c-fd44-e053-dadaa90aa01bUltra Defense Advanced Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
77618-001-01Ultra Defense Advanced Hand Sanitizer200 L in 1 DRUMGEL2002
77618-001-02Ultra Defense Advanced Hand Sanitizer0.25 L in 1 BOTTLEGEL0.252

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
77618-001ULTRA DEFENSE ADVANCED HAND SANITIZER (ALCOHOL) GEL [REPUBLIC NAIL, S.A. DE C.V.]2Legacy NDC, 2 package rows20200603_db37320c-ab13-4eca-8a42-3005fecb6e42.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
77618-00177618-001-01, 77618-001-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 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
a70c0a71-e520-6058-e053-2995a90afeb9db37320c-ab13-4eca-8a42-3005fecb6e422020-06-01WarningsExact identifier
spl id: a70c0a71-e520-6058-e053-2995a90afeb9
spl set id: db37320c-ab13-4eca-8a42-3005fecb6e42

Reported adverse events (FAERS/openFDA)#

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