Jensil Alcohol Pad

Manufacturer
YIWU HAODING MEDICAL CO.,LTD
Effective date
2023-03-03
Label type
HUMAN OTC DRUG LABEL
Version
73
Source
full-release
Hydrated at
2026-05-31 23:54:23

Label at a glance#

ProductJensil Alcohol Pad
Active ingredientALCOHOL
Label structure8 sections

Indications and uses

To remove oils and residue from skin. To Decrease germs in minor cuts and scrapes.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

DRUG FACTS

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Isopropyl Alcohol 70%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses:

INDICATIONS & USAGE SECTION

To remove oils and residue from skin.

To Decrease germs in minor cuts and scrapes.

Discard after single use.

DOSAGE & ADMINISTRATION SECTION

discard after single use.

Other Information: Room temperature storage recommended.

WARNINGS SECTION

For external use only.

Flammable, keep away from heat and flame.

Do not use: in the eyes, or over large portions of the body. In case of deep or puncture wounds, seek medical help.

OTC - STOP USE SECTION

Caustion: If skin is irritated or develops redness discontinue use and seek medical help.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If ingested, do not induce vomiting. Get medical help or contact a Poison Control Center immediately.

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Principal Display PanelPrincipal Display Panel

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69139-212-01Jensil Alcohol Pad1 in 1 PACKAGESWAB173
69139-212-01Jensil Alcohol Pad0.3 g in 1 PACKAGESWAB0.373

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69139-212JENSIL ALCOHOL PAD (ALCOHOL) SWAB [YIWU HAODING MEDICAL CO.,LTD]73Legacy NDC, 2 package rows20230307_e946cfce-861a-4d38-bffd-8c1d89757d4d.zip

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
69139-21269139-212-01

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
ALCOHOL3K9958V90MACTIB

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
f60c626d-78e3-5903-e053-2a95a90abf25e946cfce-861a-4d38-bffd-8c1d89757d4d2023-03-03WarningsExact identifier
spl id: f60c626d-78e3-5903-e053-2a95a90abf25
spl set id: e946cfce-861a-4d38-bffd-8c1d89757d4d

Reported adverse events (FAERS/openFDA)#

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