Nu-HS2 Instant hand sanitizer - 80% ethanol

Manufacturer
InnuScience Group Inc. | 1490290 Ontario Inc.
Effective date
2020-05-19
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:29:05

Label at a glance#

ProductNu-HS2 Instant hand sanitizer - 80% ethanol
Active ingredientALCOHOL
Label structure7 sections

Dosage and administration

Adults and children over 2 years: For occasional and personal household use. Rub well for at least 30 seconds. Let dry. Supervise children when using this product.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 80% v/v.

Directions

DOSAGE & ADMINISTRATION SECTION

Adults and children over 2 years: For occasional and personal household use. Rub well for at least 30 seconds. Let dry. Supervise children when using this product.

Warnings

WARNINGS SECTION

Stop use and consult a health care practitioner if irritation develops.

Flammable, keep away from flames and heat sources.

When using this product avoid contact with eyes. If necessary, rinse well with water.

For external use only.

CONTRAINDICATIONS

Do not use on children / infants under 2 years of age (except on the advice of health professional).

Other information
Store at cool place

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of the reach of children. If swallowed, call a Poison Control Center immediately or get medical assistance.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, hydrogen peroxide. This product does not contain mercury.

QUESTIONS? 1 866 922-4666

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label2Label2

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78119-00278119-002-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 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
cdc99b29-4b61-ed32-e053-2995a90a2858d3ce9f34-139c-4b06-9175-0e4471decdc02021-10-07WarningsExact identifier
spl set id: d3ce9f34-139c-4b06-9175-0e4471decdc0

Reported adverse events (FAERS/openFDA)#

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