BLUZEN HAND SANITIZER GEL–MINT

Manufacturer
Remcoda, Llc
Effective date
2020-09-11
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:29:24

Label at a glance#

ProductBLUZEN HAND SANITIZER MINT
Active ingredientALCOHOL
Label structure10 sections

Dosage and administration

■ place enough product in your palm to thoroughly cover your hands ■ rub hands together briskly until dry ■ supervise children under 6 years of age when using this product to avoid swallowing.

Storage and handling

■ Store below 110°F (43°C)

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 70% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

INDICATIONS & USAGE SECTION

Uses ■ hand sanitizer to help reduce bacteria on skin

Warnings

WARNINGS SECTION

Flammable, keep away from fire/flame

For external use only

When using this product ■ do not get into eyes. In case of contact, rinse eyes thoroughly with water

■ do not inhale or ingest

Stop use and ask a doctor if irritation and redness develop

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 right away.

Directions

DOSAGE & ADMINISTRATION SECTION

■ place enough product in your palm to thoroughly cover your hands

■ rub hands together briskly until dry

■ supervise children under 6 years of age when using this product to avoid swallowing.

Other information

STORAGE AND HANDLING SECTION

■ Store below 110°F (43°C)

Inactive ingredients

INACTIVE INGREDIENT SECTION

glycerin, hydrogen peroxide, purified water, polyethylene glycol, carbomer copolymer, fragrance

OTC - QUESTIONS SECTION

Questions? 1-800-777-1603

SPL UNCLASSIFIED SECTION

CLEANSING FORMULA

KILLS 99.9% OF GERMS

MADE IN THE USA

SULFATE FREE PARABEN FREE

VEGAN, CRUELTY FREE

SHOPBLUZEN.COM

Distributed by: Remcoda, LLC, New York, NY, 10018

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PackagingPackaging

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

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
5eb9f24b-9328-475e-af0a-18021935eb6aProduct name120180220

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
79200-802-162022-01-28C16284748780-1d6a99b39-e1e4-a426-e053-dadaa90af4c2BLUZEN HAND SANITIZER GEL–MINT

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79200-802-16BLUZEN HAND SANITIZER MINT500 mL in 1 BOTTLE, PUMPGEL5001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79200-802BLUZEN HAND SANITIZER MINT (ETHYL ALCOHOL) GEL [REMCODA, LLC]1Legacy NDC, 1 package rows20200916_873d61d0-f6ad-402d-8f91-bfaf11d1ec74.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
79200-80279200-802-16

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
38594482-0e46-49b0-bcd7-05a9dc1734c4873d61d0-f6ad-402d-8f91-bfaf11d1ec742020-09-11WarningsExact identifier
spl id: 38594482-0e46-49b0-bcd7-05a9dc1734c4
spl set id: 873d61d0-f6ad-402d-8f91-bfaf11d1ec74

Reported adverse events (FAERS/openFDA)#

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