FDA.reportPublic FDA data

HS Hand Sanitizer

Manufacturer
Nature's Own Cosmetic Company, Inc. | Nature's Own - Cosmetics Company, Inc.
Effective date
2020-10-07
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:10:15

Label at a glance#

ProductHS Hand Sanitizer
Active ingredientALCOHOL
Label structure9 sections

Dosage and administration

Place product in your palm to thoroughly cover your hand. Rub hands together briskly until dry. For occasional and personal domestic use. Supervise children under 6 years of age when using this product.

Storage and handling

Store between 15-30C (59-86F) Avoid freezing and excessive heat above 40C (104F). May discolor certain fabrics or surfaces.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% v/v.

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

Effective in destroying (harmful) bacteria to provide antiseptic cleansing.

Use

RECENT MAJOR CHANGES SECTION

Effective in destroying (harmful) bacteria to provide antiseptic cleansing.

Warnings

WARNINGS SECTION

For external use only.

Flammable.

Keep away from heat or flames and sources of heat.

When using this product, avoid contact with eyes. If contact occurs, rinse thoroughly with water.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Centre right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Place product in your palm to thoroughly cover your hand. Rub hands together briskly until dry.

For occasional and personal domestic use.

Supervise children under 6 years of age when using this product.

Other information

STORAGE AND HANDLING SECTION

Store between 15-30C (59-86F)

Avoid freezing and excessive heat above 40C (104F).

May discolor certain fabrics or surfaces.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aloe Barbadensis Leaf Juice, Carbomer, dl-alpha Tocopheryl Acetate, Glycerin, Isopropyl Alcohol, Triethanolamine, Water/Aqua/Eau.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1L label1L label1L NDC: 73756-004-01

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
73756-00473756-004-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
ISOPROPYL ALCOHOLND2M416302IACT
GLYCERINPDC6A3C0OXIACT
TROLAMINE9O3K93S3TKIACT
WATER059QF0KO0RIACT
CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED)4Q93RCW27EIACT
.ALPHA.-TOCOPHEROL ACETATE, DL-WR1WPI7EW8IACT
ALOE VERA LEAFZY81Z83H0XIACT
ALCOHOL3K9958V90MACTIB

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
b2d5a869-e3f8-7fc3-e053-2995a90adec7b220f10a-712d-9d66-e053-2a95a90a3cee2020-10-29WarningsExact identifier
spl set id: b220f10a-712d-9d66-e053-2a95a90a3cee

Reported adverse events (FAERS/openFDA)#

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