Dr. Odin ANTISEPTIC HAND SANITIZER

Manufacturer
LENUS LIFE CARE PRIVATE LIMITED
Effective date
2020-04-11
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:06:06

Label at a glance#

ProductDr. Odin ANTISEPTIC HAND SANITIZER
Active ingredientISOPROPYL ALCOHOL
Label structure10 sections

Indications and uses

• hand sanitizer to decrease bacteria on the skin • recommended for repeated use • for use when soap and water are not available

Dosage and administration

• wet hands thoroughly with product and allow to dry without wiping • supervise children under 6 years of age when using this product to avoid swallowing

Storage and handling

• store between 15-30°C (59-86°F) • avoid freezing and excessive heat above 40°C (104°F)

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Isopropyl alcohol 75% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

• hand sanitizer to decrease bacteria on the skin • recommended for repeated use • for use when soap and water are not available

Warnings

WARNINGS SECTION

Flammable, keep away from fire/flame

For external use only

Do not use • in children less than 2 months of age • on open skin wounds

When using this product • do not get into eyes. In case of contact, rinse eyes thoroughly with water

Stop use and ask a doctor if • irritation and redness develop • condition persists for more than 72 hours

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 right away.

Directions

DOSAGE & ADMINISTRATION SECTION

• wet hands thoroughly with product and allow to dry without wiping • supervise children under 6 years of age when using this product to avoid swallowing

Other information

STORAGE AND HANDLING SECTION

• store between 15-30°C (59-86°F) • avoid freezing and excessive heat above 40°C (104°F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, glycerin, carbomer, aloe vera, fragrance, triethanolamine

Questions? +1-703-255-9000

OTC - QUESTIONS SECTION

You may also report serious side effects to this phone number. Mon-Fri 9:00 AM - 5:00 PM

SPL UNCLASSIFIED SECTION

Feel Fresh & Clean

Manufactured by: Lenus Lifecare Pvt.Ltd. Plot No.1, Industrial Area, Chambaghat, Solan, H.P. India - 173213

COUNTRY OF ORIGIN: INDIA

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Odinsntz1Odinsntz1

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1039900isopropyl alcohol 75 % Topical SolutionPSN1
1039900isopropyl alcohol 0.75 ML/ML Topical SolutionSCD1
1039900isopropyl alcohol 75 % Topical SolutionSY1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1Product name120230829

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73820-110-012022-01-28C16284748780-1d6a99b39-bd90-a426-e053-dadaa90af4c2Dr. Odin ANTISEPTIC HAND SANITIZER

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73820-110-01Dr. Odin ANTISEPTIC HAND SANITIZER100 mL in 1 BOTTLE, PLASTICLIQUID1001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73820-110DR. ODIN ANTISEPTIC HAND SANITIZER (ISOPROPYL ALCOHOL) LIQUID [LENUS LIFE CARE PRIVATE LIMITED]1Legacy NDC, 1 package rows20200414_453fa7ee-bb71-445a-ab3d-2d14efe265ba.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73820-11073820-110-01

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
bdd5c9b1-a9e3-4707-ae4e-1e2841dab587453fa7ee-bb71-445a-ab3d-2d14efe265ba2020-04-11WarningsExact identifier
spl id: bdd5c9b1-a9e3-4707-ae4e-1e2841dab587
spl set id: 453fa7ee-bb71-445a-ab3d-2d14efe265ba

Reported adverse events (FAERS/openFDA)#

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