Kunigel Moisturizing Antiseptic Hand Sanitizer

Manufacturer
Setric Best, S. de R.L. de C.V.
Effective date
2022-03-31
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:49:01

Label at a glance#

ProductKunigel Moisturizing Antiseptic Hand Sanitizer
Active ingredientALCOHOL
Label structure8 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

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

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • irritation and redness develop
  • condition persists for more than 72 hours

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

Wet hands thoroughly with product and allow to dry without wiping

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, glycerin, carbomer

Package Labeling: 3.79L

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

Package Labeling: 20L

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label2Label2

Package Labeling: 200L

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label3Label3

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN2
581662ethanol 0.7 ML/ML Topical GelSCD2
581662ethanol 70 % Topical GelSY2
581662ethyl alcohol 70 % Topical GelSY2

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
81941-000-00Kunigel Moisturizing Antiseptic Hand Sanitizer3790 mL in 1 CONTAINERGEL37902
81941-000-02Kunigel Moisturizing Antiseptic Hand Sanitizer20000 mL in 1 CONTAINERGEL200002
81941-000-20Kunigel Moisturizing Antiseptic Hand Sanitizer200000 mL in 1 CONTAINERGEL2000002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
81941-000KUNIGEL MOISTURIZING ANTISEPTIC HAND SANITIZER (ALCOHOL) GEL [SETRIC BEST, S. DE R.L. DE C.V.]2Legacy NDC, 3 package rows20220401_c3b4c339-d6a7-3ce1-e053-2a95a90ae18d.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
81941-00081941-000-00, 81941-000-02, 81941-000-20

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 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
db87370b-f0b1-67ac-e053-2995a90a9f4bc3b4c339-d6a7-3ce1-e053-2a95a90ae18d2022-03-31WarningsExact identifier
spl id: db87370b-f0b1-67ac-e053-2995a90a9f4b
spl set id: c3b4c339-d6a7-3ce1-e053-2a95a90ae18d

Reported adverse events (FAERS/openFDA)#

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