FDA.reportPublic FDA data

MARTIN PRODUCE HAND SANITIZER

Manufacturer
Martin Produce, Inc.
Effective date
2020-06-04
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:18:46

Label at a glance#

ProductMARTIN PRODUCE HAND SANITIZER
Active ingredientALCOHOL
Label structure9 sections

Dosage and administration

Put enough product in your palm to cover hands and rub hands together briskly until dry. Children under 6 years of age should be supervised when using.

Storage and handling

Store below 110°F (43°C)

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% v/v

Purpose

OTC - PURPOSE SECTION

Antimicrobial

INDICATIONS & USAGE SECTION

Use: Hand sanitizer to help reduce bacteria on skin.

Warnings:

WARNINGS SECTION

Flammable. Keep away from fire or flame.

For external use only.

When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation or rash appears and lasts.

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.

Directions:

DOSAGE & ADMINISTRATION SECTION

Put enough product in your palm to cover hands and rub hands together briskly until dry.
Children under 6 years of age should be supervised when using.

Other information:

STORAGE AND HANDLING SECTION

Store below 110°F (43°C)

INACTIVE INGREDIENT SECTION

Inactive ingredients: Water (Aqua), Aloe Barbadensis Leaf Juice, Isopropyl Alcohol, Glycerin, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol

SPL UNCLASSIFIED SECTION

MADE WITH PLANT EXTRACTS AND SKIN CONDITIONERS

HIGH POTENCY 70% ALCOHOL FORMULA

DISTRIBUTED BY:

MARTIN PRODUCE

143 W 154th Street

South Holland, IL 60473

PHONE: 708-825-1519

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Mrtn1Mrtn1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
78566-100-012024-12-12C16284748780-1c7ccaba7-1f92-fd44-e053-dadaa90aa01bMARTIN PRODUCE HAND SANITIZER
78566-100-012021-07-23C16284748780-1c7ccaba7-1f92-fd44-e053-dadaa90aa01bMARTIN PRODUCE HAND SANITIZER

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78566-10078566-100-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
ALOE VERA LEAFZY81Z83H0XIACT
ISOPROPYL ALCOHOLND2M416302IACT
GLYCERINPDC6A3C0OXIACT
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)59TL3WG5COIACT
AMINOMETHYLPROPANOLLU49E6626QIACT

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
8304ffb7-05e4-43cb-b6c0-7d15e24617efe0895059-87cf-48d5-b5a6-133c864a3d952024-12-11WarningsExact identifier
spl set id: e0895059-87cf-48d5-b5a6-133c864a3d95

Reported adverse events (FAERS/openFDA)#

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