Protz ANTIBACTERIAL HAND SANITIZER

Manufacturer
MYM Hidrominerales, S, de R.L. de C.V.
Effective date
2020-05-18
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:15:34

Label at a glance#

ProductProtz ANTIBACTERIAL HAND SANITIZER
Active ingredientALCOHOL
Label structure9 sections

Storage and handling

Other information: Store below 110°F (43°C). May discolor certain fabrics or surfaces.

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Ethyl alcohol 70% v/v

OTC - PURPOSE SECTION

Purpose

Antimicrobial

INDICATIONS & USAGE SECTION

Use: Hand sanitizer to help reduce bacteria on the skin.

WARNINGS SECTION

Warnings

Flammable. Keep away from fire or flame. For external use only.

Do not ingest, if swallowed seek medical help. Avoid contact with eyes.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. Children under 6yrs old to use under adult supervision. In case of irritation, discontinue use and consult your doctor.

DOSAGE & ADMINISTRATION SECTION

Directions: Apply the Gel on the hands and rub gently for 20 seconds until the product evaporates.

STORAGE AND HANDLING SECTION

Other information: Store below 110°F (43°C). May discolor certain fabrics or surfaces.

INACTIVE INGREDIENT SECTION

Inactive ingredients: Water (Aqua), Glycerin, Aminomethylpropanol, Carbomer, Propylene Glycol.

SPL UNCLASSIFIED SECTION

real protection

ELIMINATES 99% OF GERMS AND BACTERIA

EcoPure®

Enhanced Bottle

 ✓ MOISTURIZING

   ✓ WITHOUT RINSING

✓ FAMILY USE

Protz alcohol gel is a natural antiseptic and disinfectant that kills common germs without water or a hand towel. Its immediate action provides a special decontaminating action on the skin and dirty surfaces.

Distributed by:

Safety-Med Products, Inc. Burlington, WI 53105.

www.safety-med.com

Phone N   umber: 222 95 22 453

MADE IN MEXICO BY MYM HIDROMINERALES S. DE R.L. DE C.V.

Address: AV. 5 DE MAYO 600 C, CHIPILO, PUEBLA, C.P. 74325

Batch and expiration on the packaging

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
77872-600-402021-07-23C16284748780-1c7ccaba7-1eba-fd44-e053-dadaa90aa01bProtz ANTIBACTERIAL HAND SANITIZER

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
77872-600-40Protz ANTIBACTERIAL HAND SANITIZER400 mL in 1 BOTTLEGEL4001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
77872-600PROTZ ANTIBACTERIAL HAND SANITIZER (ETHYL ALCOHOL) GEL [MYM HIDROMINERALES, S, DE R.L. DE C.V.]1Legacy NDC, 1 package rows20200601_bd1a573f-04e8-48a2-9878-e1f5ba85a468.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
77872-60077872-600-40

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
0dcd816c-66f6-4060-aec9-472fa7a4a191bd1a573f-04e8-48a2-9878-e1f5ba85a4682020-05-18WarningsExact identifier
spl id: 0dcd816c-66f6-4060-aec9-472fa7a4a191
spl set id: bd1a573f-04e8-48a2-9878-e1f5ba85a468

Reported adverse events (FAERS/openFDA)#

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