KO-KING EPISODE ONE

Manufacturer
JNJ COSTEC CO
Effective date
2020-11-24
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:34:13

Label at a glance#

ProductKO-KING EPISODE ONE
Active ingredientALCOHOL
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Alcohol

INACTIVE INGREDIENT SECTION

Water
Glycerin
PEG-60 Hydrogenated Castor Oil
Carbomer
Triethanolamine
Sodium Hyaluronate
Tocopherol
Butylene Glycol
1,2-Hexanediol

ETC

OTC - PURPOSE SECTION

Instantly kils most common germs and bacteria without damaging skin and stop some viruses.
Great alternative when soap and water are not available.
Disposable and quick-drying.
Perfect and convenient to carry in purse, school backpacks and travel bags.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF THE CHILDREN

INDICATIONS & USAGE SECTION

Just apply it, let it dry a few seconds. No water or towels needed.

WARNINGS SECTION

1. Do not use this product on the following parts of body. Around eyes and ears, oral cavity, large area of the
parts of body, or wounded skins (It may cause irritations)
2. Stop using at once in case of the following symptoms, and seek medical advice. 1) When eczema, red spots,
itchiness, edema, and allergic reactions occur. 2)When skin irritations happen.
3. Other user reminders 1) For external use only(No oral intake). 2) Avoid contact with eyes, and in case contact
occurs, rinse it thoroughly with clean water and consult a doctor or pharmacist. 3) When you use it on a large skin
area or use it long-termly, please be aware that vapor is not absorbed. (If Ethanol vapor is largely and repeatedly
inhaled and absorbed, it may cause irritation to mucous membrane and headache might occur.) 4)When the product
is used on the same part of skin repeatedly, the skin may become rough due to skimming. 5) Do not use with sealed
gauze bandage, Gibbs bandage or pack, as irritations may occur. 6) Do not use this product while anus and vagina
steaming as irritations or chemical burns may occur. 7) Do not use for purposes other than specified.

DOSAGE & ADMINISTRATION SECTION

external use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LABELLABEL

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581660ethanol 62 % Topical GelPSN1
581660ethanol 0.62 ML/ML Topical GelSCD1
581660ethanol 62 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
78488-0005-12022-01-28C16284748780-1d6a99b39-e6e7-a426-e053-dadaa90af4c2Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
78488-0005-1KO-KING EPISODE ONE500 mL in 1 BOTTLEGEL5001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
78488-0005KO-KING EPISODE ONE (ALCOHOL) GEL [JNJ COSTEC CO]1Legacy NDC, 1 package rows20201125_b4d81ec8-c65e-9bf9-e053-2995a90aa5b5.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78488-000578488-0005-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 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
b4d7fe59-a078-757c-e053-2995a90aaf0bb4d81ec8-c65e-9bf9-e053-2995a90aa5b52020-11-24WarningsExact identifier
spl id: b4d7fe59-a078-757c-e053-2995a90aaf0b
spl set id: b4d81ec8-c65e-9bf9-e053-2995a90aa5b5

Reported adverse events (FAERS/openFDA)#

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