Helios Hand Sanitizer Gel 80 mL

Manufacturer: Pretty Woman LLC
Effective date: 2020-05-21
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:13:59

Label at a glance#

ProductHELIOS Hand Sanitizer

Active ingredientALCOHOL

Label structure11 sections

Dosage and administration

Directions wet hands thoroughly with product and allow to dry without wiping for children under 6 years of age, use only under adult supervision not recommended for infants

Storage and handling

Other information store below 104ºF (40ºC) may discolor certain fabrics or surfaces

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 75% v/v. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer

Use

INDICATIONS & USAGE SECTION

to decrease bacteria on the skin that could cause disease
recommended for repeated use

Warnings

WARNINGS SECTION

For external use only: hands. Flammable. Keep away from fire or flame.

OTC - WHEN USING SECTION

When using this product

keep out of eyes. In case of contact with eyes, flush thoroughly with water.
avoid contact with broken skin
do not inhale or ingest

OTC - STOP USE SECTION

Stop use and ask a doctor if

irritation or redness develops
conditions persists more that 72h

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

Directions

wet hands thoroughly with product and allow to dry without wiping
for children under 6 years of age, use only under adult supervision
not recommended for infants

Other information

STORAGE AND HANDLING SECTION

Other information

store below 104ºF (40ºC)
may discolor certain fabrics or surfaces

Inactive ingredients

INACTIVE INGREDIENT SECTION

acrylates copolymer, aminomethyl propanol, fragrance, glycerin, water

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label HHS19 80ml PDPLabel HHS19 80ml INSIDELabel HHS19 80ml BASE80 mL NDC: 74140-200-01

Product Linked Resources#

Resource, Code type, Value table
Resource	Code type	Value	Equivalent identifiers	Source image
Barcode	EAN-13	0800307804895	GTIN-13: 0800307804895 EAN-13: 0800307804895 GTIN-12: 800307804895 UPC-A: 800307804895 GTIN storage (14 digits): 00800307804895	Label HHS19 80ml PDP.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
74140-200-01	2022-01-28	C162847	48780-1	d6a99b39-d940-a426-e053-dadaa90af4c2	Helios Hand Sanitizer Gel 80 mL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
74140-200-01	HELIOS Hand Sanitizer	80 mL in 1 BOTTLE, PLASTIC	GEL	80		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
74140-200	HELIOS HAND SANITIZER (ALCOHOL) GEL [PRETTY WOMAN LLC]	1	Legacy NDC, 1 package rows	20200521_a61327b9-09e9-3887-e053-2a95a90ab0f0.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

HELIOS Hand Sanitizer
ALCOHOL
WATER
AMINOMETHYLPROPANOL
GLYCERIN
BUTYL ACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID COPOLYMER (18000 MW)

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
74140-200	74140-200-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
AMINOMETHYLPROPANOL	LU49E6626Q	IACT
GLYCERIN	PDC6A3C0OX	IACT
BUTYL ACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID COPOLYMER (18000 MW)	JZ1374NL9E	IACT
ALCOHOL	3K9958V90M	ACTIB

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
a61327b9-09ea-3887-e053-2a95a90ab0f0			a61327b9-09e9-3887-e053-2a95a90ab0f0	2020-05-21	Warnings	Exact identifier spl id: a61327b9-09ea-3887-e053-2a95a90ab0f0 spl set id: a61327b9-09e9-3887-e053-2a95a90ab0f0

Reported adverse events (FAERS/openFDA)#

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