Koi Hand Sanitizer

Manufacturer
Koi CBD LLC | Brad Ridenour
Effective date
2020-08-03
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:23:34

Label at a glance#

ProductKoi Hand Sanitizer
Active ingredientALCOHOL
Label structure11 sections

Storage and handling

Do not store about 110°F. Harmful to wood finishes and plastics.

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70%...... Antimicrobial

OTC - PURPOSE SECTION

Antimicrobial

INDICATIONS & USAGE SECTION

Hand sanitizer to help decrease bacteria on the skin. Recommended for repeat use.

WARNINGS SECTION

For external use only. Flammable, keep away from fire or flames.

OTC - DO NOT USE SECTION

Do not use in children less than 2 months of age or on open skin wounds.

OTC - STOP USE SECTION

Stop use and consult a doctor if irritation or rash occurs. These may be signs of a serious condition.

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 immediately.

DOSAGE & ADMINISTRATION SECTION

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

STORAGE AND HANDLING SECTION

Do not store about 110°F. Harmful to wood finishes and plastics.

INACTIVE INGREDIENT SECTION

Water, Glycerin, Propylene Glycol,Carbomer, Triethanolamine, Fragrance.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 73842-003-001 Bottle 59 mL 2oz-sanitizer-2.jpg2oz-sanitizer-2.jpg

NDC 73842-003-002 Bottle 118 mL

4oz-sanitizer-2.jpg4oz-sanitizer-2.jpg

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN1
581662ethanol 0.7 ML/ML Topical GelSCD1
581662ethanol 70 % Topical GelSY1
581662ethyl alcohol 70 % Topical GelSY1

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130857321007108GTIN-13: 0857321007108
EAN-13: 0857321007108
GTIN-12: 857321007108
UPC-A: 857321007108
GTIN storage (14 digits): 00857321007108
4oz-sanitizer-2.jpg
BarcodeEAN-130857321007207GTIN-13: 0857321007207
EAN-13: 0857321007207
GTIN-12: 857321007207
UPC-A: 857321007207
GTIN storage (14 digits): 00857321007207
2oz-sanitizer-2.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73842-003-012022-01-28C16284748780-1d6a99b39-f961-a426-e053-dadaa90af4c2Koi Hand Sanitizer
73842-003-022022-01-28C16284748780-1d6a99b39-f961-a426-e053-dadaa90af4c2Koi Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73842-003-01Koi Hand Sanitizer59 mL in 1 BOTTLEGEL591
73842-003-02Koi Hand Sanitizer118 mL in 1 BOTTLEGEL1181

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73842-003KOI HAND SANITIZER (ETHYL ALCOHOL, 70%) GEL [KOI CBD LLC]1Legacy NDC, 2 package rows20200803_abc1264b-1a0d-bec3-e053-2995a90a0df5.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73842-00373842-003-01, 73842-003-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 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
abc0d09a-614c-cfcb-e053-2a95a90af8bdabc1264b-1a0d-bec3-e053-2995a90a0df52020-08-03WarningsExact identifier
spl id: abc0d09a-614c-cfcb-e053-2a95a90af8bd
spl set id: abc1264b-1a0d-bec3-e053-2995a90a0df5

Reported adverse events (FAERS/openFDA)#

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