Jermee Hand Sanitizer

Manufacturer
Jermee Inc
Effective date
2023-01-05
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 21:41:42

Label at a glance#

ProductJermee Hand Sanitizer
Active ingredientALCOHOL
Label structure7 sections

Indications and uses

Hand sanitizer to help reduce bacteria on the skin that may cause disease.

Dosage and administration

Apply small amount of product, rubbing hands thoroughly with product until dry. No rinsing needed. Children under 6 years of age should be supervised when using this product.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70%

Purpose

OTC - PURPOSE SECTION

Anti Microbial

Uses

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria on the skin that may cause disease.

Warnings:

WARNINGS SECTION

Flammable. Keep away from fire or flame.

For external use only.

When using this product

OTC - WHEN USING SECTION

Do not use in eyes. In case of contact with eyes, rinse with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

irritation or redness develops.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help promptly.

Directions

DOSAGE & ADMINISTRATION SECTION

Apply small amount of product, rubbing hands thoroughly with product until dry. No rinsing needed. Children under 6 years of age should be supervised when using this product.

Other Information

SPL UNCLASSIFIED SECTION

Store under 105 F.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Isopropyl Alcohol, Glycerine, Carbomer, Fragrance

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BottleBottle

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
78573-002JERMEE HAND SANITIZER (ALCOHOL) GEL [JERMEE INC]3Legacy NDC20230106_49ae5550-c778-4221-a99d-d28cc2a4099c.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78573-00278573-002-00

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 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
f187d890-3909-8614-e053-2a95a90ab91d49ae5550-c778-4221-a99d-d28cc2a4099c2023-01-05WarningsExact identifier
spl id: f187d890-3909-8614-e053-2a95a90ab91d
spl set id: 49ae5550-c778-4221-a99d-d28cc2a4099c

Reported adverse events (FAERS/openFDA)#

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