MedPRIDE

Manufacturer
Shield Line LLC
Effective date
2026-03-17
Label type
HUMAN OTC DRUG LABEL
Version
9
Source
full-release
Hydrated at
2026-06-01 01:50:38

Label at a glance#

ProductMedPRIDE
Active ingredientISOPROPYL ALCOHOL
Label structure12 sections

Indications and uses

first aid to help prevent risk of infection in  minor cuts, scrapes and burns

Dosage and administration

■ clean affected area ■ apply a small amount of this product on the area 1 to 3 times daily ■ if bandaged, let dry first ■ may be covered with a sterile bandage

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Isopropyl Alcohol 70%

Purpose

OTC - PURPOSE SECTION

First Aid Antiseptic

Uses

INDICATIONS & USAGE SECTION

first aid to help prevent risk of infection in  minor cuts, scrapes and burns

Warnings

WARNINGS SECTION

For external use only

■ Flammable, keep away from fire and flame

■ if taken internally, serious gastric disturbances will result

Ask a doctor before use if you have

OTC - ASK DOCTOR SECTION

■ deep or puncture wounds, animal bites or serious burns

When using this product

OTC - WHEN USING SECTION

■ do not get into your eyes ■ do not apply over large areas of the body ■ do not use longer than one week unless directed by a doctor

■ do not use otherwise than directed

Stop use and ask a doctor if

OTC - STOP USE SECTION

■ condition persists or gets worse

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of ingestion, get medical help or contact a Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

■ clean affected area ■ apply a small amount of this product on the area 1 to 3 times daily

■ if bandaged, let dry first ■ may be covered with a sterile bandage

Other information

OTHER SAFETY INFORMATION

■ store at room temperature

■ does not contain nor is intended as a substitute for grain or ethyl alcohol

Inactive Ingredient

INACTIVE INGREDIENT SECTION

purified water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

MdPrdIsprpylAlcMdPrdIsprpylAlc

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130352410409639GTIN-13: 0352410409639
EAN-13: 0352410409639
GTIN-12: 352410409639
UPC-A: 352410409639
GTIN storage (14 digits): 00352410409639
MdPrdIsprpylAlc.jpg

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
52410-4096-3MedPRIDE355 mL in 1 BOTTLE, PLASTICLIQUID3559
52410-4096-5MedPRIDE475 mL in 1 BOTTLE, PLASTICLIQUID4759
52410-4096-7MedPRIDE946.3 mL in 1 BOTTLELIQUID946.39

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ISOPROPYL ALCOHOLACTIVE INGREDIENTND2M4163021
ISOPROPYL ALCOHOLACTIVE MOIETYND2M4163021
WATERINACTIVE INGREDIENT059QF0KO0R1

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
52410-409652410-4096-3, 52410-4096-5, 52410-4096-7

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
ISOPROPYL ALCOHOLND2M416302ACTIB

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
MedPRIDEISOPROPYL ALCOHOLShield Line LLCf2177bd3-259d-4231-88b2-4a98e48e4df62026-03-17WarningsExact identifier
ndc (package): 52410-4096-5
ndc (package): 52410-4096-3
ndc (package): 52410-4096-7
ndc (product): 52410-4096
ndc11 (package): 52410409605
ndc11 (package): 52410409607
ndc11 (package): 52410409603
spl id: 4d3bd829-fe87-0611-e063-6294a90ae57c
spl set id: f2177bd3-259d-4231-88b2-4a98e48e4df6

Reported adverse events (FAERS/openFDA)#

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