Hand Sanitizer

Manufacturer
Nature’s Own Cosmetics Company Inc.
Effective date
2020-10-21
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:10:06

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure8 sections

Dosage and administration

Rub thoroughly into hands for at least 30 seconds. Allow to dry. For occasional and personal domestic use. Supervise children when they use this product. For children 2 to 11 years, Adolescents 12 to 17 years, Adults 18 years and older. Other Information: Store below 100 F (43 C). May discolor certain fabrics or surfaces.

Label contents#

Full prescribing information#

Medicinal Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% v/v.

Purpose

OTC - PURPOSE SECTION

Antiseptic

Warnings

WARNINGS SECTION

For external use only. When using this product, avoid contact with eyes. If contact occurs, rinse thoroughly with water. Stop use and ask/consult a doctor /physician /health care practitioner/health care professional if irritation develops.

Keep away from open flame and sources of heat.

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

Rub thoroughly into hands for at least 30 seconds. Allow to dry. For occasional and personal domestic use. Supervise children when they use this product. For children 2 to 11 years, Adolescents 12 to 17 years, Adults 18 years and older.

Other Information: Store below 100 F (43 C). May discolor certain fabrics or surfaces.

Non-Medicinal Ingredients

INACTIVE INGREDIENT SECTION

Water, lsopropanol, Ethyl Acetate, Glycerin, Carbomer, Triethanolamine, Aloe Barbadensis leaf Juice, dl-alpha Tocopheryl Acetate.

Product Labels

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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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
73756-00273756-002-01, 73756-002-02, 73756-002-03, 73756-002-04, 73756-002-05

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 · 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
b231204d-38cb-dbc9-e053-2a95a90a436f2df540af-77b5-4b41-bdd2-237f1d949a912020-10-21WarningsExact identifier
spl id: b231204d-38cb-dbc9-e053-2a95a90a436f
spl set id: 2df540af-77b5-4b41-bdd2-237f1d949a91

Reported adverse events (FAERS/openFDA)#

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