MIUS

Manufacturer
MIUS Industries Corp.
Effective date
2017-12-26
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:54:10

Label at a glance#

ProductMIUS
Active ingredientALCOHOL
Label structure7 sections

Indications and uses

■ Helps reduce bacteria on the skin ■ Recommended for repeated use

Dosage and administration

■ Shake well before use due to natural separation ■ Spray directly on hands and rub thoroughly ■ For children under 6, use adult supervision ■ Not recommended for infants

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

■ Helps reduce bacteria on the skin

■ Recommended for repeated use

Warning

WARNINGS SECTION

For External use only

Flammable, keep away from fire, sparks, and sources of ignition.

WARNINGS AND PRECAUTIONS SECTION

Do not store above 104° F/ 40° C

When using this product

OTC - WHEN USING SECTION

■ Keep out of eyes ■ In case of contact with eyes flush thoroughly with water ■ Avoid contact with broken skin

Stop use and ask a doctor if

OTC - STOP USE SECTION

irritation and redness develop and persist for more than 72 hours

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed get medical help or contact a Poison Control Center immediately

Directions

DOSAGE & ADMINISTRATION SECTION

■ Shake well before use due to natural separation ■ Spray directly on hands and rub thoroughly ■ For children under 6, use adult supervision ■ Not recommended for infants

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Apple Cider Vinegar, Vegetable Glycerin, Vitamin E Safflower Oil

MIUS Natural Hand Sanitizer Free and Clear

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

MIUS Stamp Free and Clear Jpeg.jpgMIUS Stamp Free and Clear Jpeg.jpgFree and clear back label.jpgFree and clear back label.jpg

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1041849ethanol 70 % Topical SprayPSN1
1041849ethanol 0.7 ML/ML Topical SpraySCD1
1041849ethanol 70 % Topical SpraySY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71887-272-022020-01-31C16284748780-19d75b9d0-9c40-f424-e053-dadaa90a57ceMIUS Hand Sanitizer Free and Clear

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71887-272-02MIUS60 mL in 1 BOTTLE, SPRAYSPRAY601

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71887-272MIUS (ETHYL ALCOHOL) SPRAY [MIUS INDUSTRIES CORP.]1Legacy NDC, 1 package rows20180119_61490ad7-143d-8c77-e053-2991aa0a1521.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
71887-27271887-272-02

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
61490ad7-143e-8c77-e053-2991aa0a152161490ad7-143d-8c77-e053-2991aa0a15212017-12-26WarningsExact identifier
spl id: 61490ad7-143e-8c77-e053-2991aa0a1521
spl set id: 61490ad7-143d-8c77-e053-2991aa0a1521

Reported adverse events (FAERS/openFDA)#

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