FDA.reportPublic FDA data

MediPlus

Manufacturer
LIX DETERGENT JOINT STOCK COMPANY
Effective date
2020-04-29
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:10:17

Label at a glance#

ProductMediPlus
Active ingredientALCOHOL
Label structure9 sections

Storage and handling

Other information  (i) store between 15-30C (59-86F) (ii) avoid freezing and excessive heat above 40C (104F)

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient [s]: Alcohol 70% v/v

OTC - PURPOSE SECTION

Purpose: Antiseptic

INDICATIONS & USAGE SECTION

Use [s]: Hand Sanitizer to help reduce bacteria that potentially can cause disease. Use when soap and water are not available.

WARNINGS SECTION

Warnings: For external use only. Flammable. Keep away from heat or flame.

Do not use (i) in children less than 2 months of age (ii) on open skin wounds

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse thoroughly with water.

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

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.

DOSAGE & ADMINISTRATION SECTION

Directions (i) Place enough product on hands to cover all surfaces. Rub hands together until dry (ii) Supervise children under 6 years of age when using this product to avoid swallowing.

STORAGE AND HANDLING SECTION

Other information (i) store between 15-30C (59-86F) (ii) avoid freezing and excessive heat above 40C (104F)

INACTIVE INGREDIENT SECTION

Inactive ingredients: water, glycerin, carbomer, aminomethyl propanol, perfume

SPL UNCLASSIFIED SECTION

WITHOUT WATER

CONTAINS 70% Alcohol

FIRST AID: If swelling, redness, blistering or irritation occurs, seek medical assistance. If in eyes or mouth, rinse continuously with water and consult a doctor or Poisons Information Centre.

Flammable, keep away from fire or flame.

Purpose: Antiseptic

Use: To decrease bacteria on the skin and clean hands. Recommended for repeated use.

Storage information: Store in a cool, dry, well-ventilated place and out of direct sunlight.

Warning: For external use only.

Directions: Apply to hands until thoroughly wet. Rub vigorously until dry. Supervise children in the use of this product. This is not a toy.

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PackagingPackaging

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
582753ethanol 70 % Topical SolutionPSN1
582753ethanol 0.7 ML/ML Topical SolutionSCD1
582753ethanol 70 % Topical SolutionSY1
582753ethyl alcohol 70 % Topical SolutionSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
76802-100-012022-01-28C16284748780-1d6a99b39-d922-a426-e053-dadaa90af4c2MediPlus INSTANT HAND SANITISER
76802-100-022022-01-28C16284748780-1d6a99b39-d922-a426-e053-dadaa90af4c2MediPlus INSTANT HAND SANITISER
76802-100-032022-01-28C16284748780-1d6a99b39-d922-a426-e053-dadaa90af4c2MediPlus INSTANT HAND SANITISER
76802-100-042022-01-28C16284748780-1d6a99b39-d922-a426-e053-dadaa90af4c2MediPlus INSTANT HAND SANITISER

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76802-100-01MediPlus100 mL in 1 BOTTLELIQUID1001
76802-100-02MediPlus250 mL in 1 BOTTLELIQUID2501
76802-100-03MediPlus500 mL in 1 BOTTLELIQUID5001
76802-100-04MediPlus1000 mL in 1 BOTTLELIQUID10001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
76802-100MEDIPLUS (ETHYL ALCOHOL) LIQUID [LIX DETERGENT JOINT STOCK COMPANY]1Legacy NDC, 4 package rows20200508_c3149f92-d8f7-4160-bc42-2acd910aeba2.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
76802-10076802-100-01, 76802-100-02, 76802-100-03, 76802-100-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
AMINOMETHYLPROPANOLLU49E6626QIACT

Source Document#

Source XML · Source PDF

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
3e0f1b13-e98d-41cb-b2bd-7ee6c8cf99aac3149f92-d8f7-4160-bc42-2acd910aeba22020-04-29WarningsExact identifier
spl id: 3e0f1b13-e98d-41cb-b2bd-7ee6c8cf99aa
spl set id: c3149f92-d8f7-4160-bc42-2acd910aeba2

Reported adverse events (FAERS/openFDA)#

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