FDA.reportPublic FDA data

Mynt Hand Sanitizers

Manufacturer
Prive International Inc.
Effective date
2020-07-16
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:21:48

Label at a glance#

ProductMynt Hand Sanitizers
Active ingredientALCOHOL
Label structure10 sections

Storage and handling

Other information: Do not store above 105°F ▪ May discolor some fabrics ▪ Harmful to wood finishes and plastics.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70%

Purpose

OTC - PURPOSE SECTION

Antiseptic

INDICATIONS & USAGE SECTION

Uses: To decrease bacteria on the skin that could cause disease  ▪ Recommended for repeated use.

WARNINGS SECTION

WARNINGS: For external use only: Hands.

FLAMMABLE, KEEP AWAY FROM FIRE OR FLAME.

When using this product ▪ Keep out of eyes. In case of contact with eyes, flush thoroughly with water

▪ Avoid contact with broken skin ▪ Do not inhale or ingest ▪ Stop use and ask a doctor if: irritation and

redness develop or condition persists for more than 72 hours.

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.

DOSAGE & ADMINISTRATION SECTION

Directions: Wet hands thoroughly with product and allow to dry without wiping ▪ For children under 6,

use only under adult supervision ▪ Not recommended for infants.

STORAGE AND HANDLING SECTION

Other information: Do not store above 105°F ▪ May discolor some fabrics ▪ Harmful to wood finishes and plastics.

INACTIVE INGREDIENT SECTION

Inactive ingredients Deionized Water, Aloe Vera Gel (Aloe Barbadensis Leaf Juice), Carbomer, Triethanolamine,

Vitamin E (Tocopheryl Acetate).

SPL UNCLASSIFIED SECTION

70% ALCOHOL

Kills 99.99% of Germs

Aloe Vera & Vitamin E

Fragrance Free

*Effective at eliminating more than 99.99% of many common harmful germs and bacteria in as little as 15 seconds.

Distributed by: Mynt Brands Miami, FL 33179

www.myntsanitizers.com - Info@myntsanitizers.com

CRUELTY FREE

VEGAN

PARABEN FREE

NO SULFATES

MADE IN USA

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PackagingPackaging

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

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#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
79442-100-022022-01-28C16284748780-1d6a99b39-abc8-a426-e053-dadaa90af4c2MYNT ® HAND SANITIZER
79442-100-042022-01-28C16284748780-1d6a99b39-abc8-a426-e053-dadaa90af4c2MYNT ® HAND SANITIZER
79442-100-082022-01-28C16284748780-1d6a99b39-abc8-a426-e053-dadaa90af4c2MYNT ® HAND SANITIZER
79442-100-122022-01-28C16284748780-1d6a99b39-abc8-a426-e053-dadaa90af4c2MYNT ® HAND SANITIZER
79442-100-162022-01-28C16284748780-1d6a99b39-abc8-a426-e053-dadaa90af4c2MYNT ® HAND SANITIZER
79442-100-282022-01-28C16284748780-1d6a99b39-abc8-a426-e053-dadaa90af4c2MYNT ® HAND SANITIZER

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79442-100-02Mynt Hand Sanitizers59 mL in 1 BOTTLEGEL592
79442-100-04Mynt Hand Sanitizers118 mL in 1 BOTTLEGEL1182
79442-100-08Mynt Hand Sanitizers237 mL in 1 BOTTLEGEL2372
79442-100-12Mynt Hand Sanitizers354 mL in 1 BOTTLEGEL3542
79442-100-16Mynt Hand Sanitizers473 mL in 1 BOTTLEGEL4732
79442-100-28Mynt Hand Sanitizers3780 mL in 1 BOTTLEGEL37802

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79442-100MYNT HAND SANITIZERS (ETHYL ALCOHOL) GEL [PRIVE INTERNATIONAL INC.]2Legacy NDC, 6 package rows20200718_58a75509-36d1-443a-99a7-70d9b9c60a67.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
79442-10079442-100-02, 79442-100-04, 79442-100-08, 79442-100-12, 79442-100-16, 79442-100-28

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
ALOE VERA LEAFZY81Z83H0XIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
TROLAMINE9O3K93S3TKIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT

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
fd2a0b14-07da-46db-b09b-0f73e6dc03c958a75509-36d1-443a-99a7-70d9b9c60a672020-07-16WarningsExact identifier
spl id: fd2a0b14-07da-46db-b09b-0f73e6dc03c9
spl set id: 58a75509-36d1-443a-99a7-70d9b9c60a67

Reported adverse events (FAERS/openFDA)#

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