MediChoice Instant Hand Sanitizer

Manufacturer
O&M HALYARD, INC.
Effective date
2025-10-08
Label type
HUMAN OTC DRUG LABEL
Version
10
Source
full-release
Hydrated at
2026-06-01 01:38:42

Label at a glance#

ProductMediChoice Instant Hand Sanitizer Fragrance free
Active ingredientALCOHOL
Label structure8 sections

Indications and uses

hand sanitizer to help reduce bacteria  on the skin

Dosage and administration

place enough product in your palm to thoroughly cover your hands rub hands together briskly until dry children under 6 years of age should be supervised when using this product not recommended for infants

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

  • hand sanitizer to help reduce bacteria  on the skin

Warnings

WARNINGS SECTION

Flammable. Keep away from fire or flame

For external use only - hands.

Do not use

OTC - DO NOT USE SECTION

in or near the eyes. In case of contact, rinse eyes thoroughly with water

Stop use and ask a doctor

OTC - STOP USE SECTION

if skin irritation and redness or rash develops.

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 right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • place enough product in your palm to thoroughly cover your hands
  • rub hands together briskly until dry
  • children under 6 years of age should be supervised when using this product
  • not recommended for infants

Other Information

SPL UNCLASSIFIED SECTION

  • store at normal room temperature 
  • may discolor certain fabrics
  • may be harmful to wood finishes and plastics

Inactive ingredients

INACTIVE INGREDIENT SECTION

Purified Water, Isopropyl Alcohol, Propylene Glycol, Aloe Barbadensis Leaf Juice (Decolorized), Carbomer, Glycerin, Aminomethyl Propanol, Isopropyl Myristate, Tocopheryl Acetate

Package Labeling: (39892-0401-2) 

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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Package Labeling: (39892-0401-3)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN10
581662ethanol 0.7 ML/ML Topical GelSCD10
581662ethanol 70 % Topical GelSY10
581662ethyl alcohol 70 % Topical GelSY10

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeData Matrix(01)10885632103322(17)170920(10)YYMMXX01AGTIN-14: 10885632103322
GTIN storage (14 digits): 10885632103322
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BarcodeData Matrix(01)10885632103339(17)170920(10)YYMMXX01AGTIN-14: 10885632103339
GTIN storage (14 digits): 10885632103339
Tube4.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
39892-0401-2MediChoice Instant Hand Sanitizer Fragrance free118 mL in 1 BOTTLEGEL11810
39892-0401-3MediChoice Instant Hand Sanitizer Fragrance free237 mL in 1 BOTTLEGEL23710

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
39892-040139892-0401-2, 39892-0401-3

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
92024-11-14full-release2026-06-01 00:37:34

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
MediChoice Instant Hand Sanitizer Fragrance freeALCOHOLO&M HALYARD, INC.c9cd6726-8a3a-429e-bef4-e0614b7540eb2025-10-08WarningsExact identifier
ndc (package): 39892-0401-3
ndc (package): 39892-0401-2
ndc (product): 39892-0401
ndc11 (package): 39892040103
ndc11 (package): 39892040102
spl id: 40b22ae5-d524-ca68-e063-6294a90a3852
spl set id: c9cd6726-8a3a-429e-bef4-e0614b7540eb

Reported adverse events (FAERS/openFDA)#

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