Hand Sanitizer

Manufacturer: Herstyler, Inc.
Effective date: 2020-05-05
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:09:50

Label at a glance#

ProductHand Sanitizer

Active ingredientALCOHOL

Label structure12 sections

Indications and uses

■ Hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available

Dosage and administration

■ Apply a dime sized amount to hands. Rub hands together until dry ■ Supervise children under 6 years of age when using this product to avoid swallowing

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 80%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

■ Hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available

Warnings

WARNINGS SECTION

For external use only. Flammable, keep away from fire and flame.

Do not use

OTC - DO NOT USE SECTION

■ on children less than 2 months of age ■ on open skin wounds

When using this product

OTC - WHEN USING SECTION

■ keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes throughly with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

irritation and redness develops and persists.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, contact a doctor or Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

■ Apply a dime sized amount to hands. Rub hands together until dry ■ Supervise children under 6 years of age when using this product to avoid swallowing

Other information

SPL UNCLASSIFIED SECTION

Store between 59-86ºF. Avoid freezing and excessive heat above 104ºF

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Acrylates Copolymer, Glycerin, Aminomethyl Propanol, Hemp (Cannabis Sativa) Seed Oil, Aloe Vera (Aloe Barbadensis) Leaf Extract, Tocopheryl Acetate (Vitamin E)

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

package label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1041498	ethanol 80 % Topical Gel	PSN	1
1041498	ethanol 0.8 ML/ML Topical Gel	SCD	1
1041498	ethanol 80 % Topical Gel	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
75177-016-01	2022-01-28	C162847	48780-1	d6a99b39-a5de-a426-e053-dadaa90af4c2	BEAUTYfrizz Hand Sanitizer
75177-016-16	2022-01-28	C162847	48780-1	d6a99b39-a5de-a426-e053-dadaa90af4c2	BEAUTYfrizz Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
75177-016-01	Hand Sanitizer	30 mL in 1 BOTTLE, PLASTIC	LIQUID	30		1
75177-016-16	Hand Sanitizer	500 mL in 1 BOTTLE, PLASTIC	LIQUID	500		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
75177-016	HAND SANITIZER (ALCOHOL) LIQUID [HERSTYLER, INC.]	1	Legacy NDC, 2 package rows	20200506_a4ee6eb7-c56f-5a2c-e053-2995a90ada10.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

Hand Sanitizer
Alcohol
CANNABIS SATIVA SEED OIL
ALOE VERA LEAF
GLYCERIN
WATER
.ALPHA.-TOCOPHEROL ACETATE
AMINOMETHYLPROPANOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
75177-016	75177-016-16, 75177-016-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
CANNABIS SATIVA SEED OIL	69VJ1LPN1S	IACT
ALOE VERA LEAF	ZY81Z83H0X	IACT
GLYCERIN	PDC6A3C0OX	IACT
WATER	059QF0KO0R	IACT
ALCOHOL	3K9958V90M	ACTIB
.ALPHA.-TOCOPHEROL ACETATE	9E8X80D2L0	IACT
AMINOMETHYLPROPANOL	LU49E6626Q	IACT

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
a4ed87ef-3466-2d44-e053-2995a90ac77c			a4ee6eb7-c56f-5a2c-e053-2995a90ada10	2020-05-05	Warnings	Exact identifier spl id: a4ed87ef-3466-2d44-e053-2995a90ac77c spl set id: a4ee6eb7-c56f-5a2c-e053-2995a90ada10

Reported adverse events (FAERS/openFDA)#

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