Hand Sanitizer

Manufacturer
Herstyler, Inc.
Effective date
2020-04-13
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:06:11

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure12 sections

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 70%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

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 wiyh 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, Glycerin, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Fragrance, Triethanolamine, Aloe Barbadensis Extract, Tocopheryl Acetate

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Package LabelPackage Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN1
581662ethanol 0.7 ML/ML Topical GelSCD1
581662ethanol 70 % Topical GelSY1
581662ethyl alcohol 70 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75177-010-01Hand Sanitizer30 mL in 1 BOTTLE, PLASTICLIQUID301
75177-010-03Hand Sanitizer100 mL in 1 BOTTLE, PLASTICLIQUID1001
75177-010-07Hand Sanitizer220 mL in 1 BOTTLE, PLASTICLIQUID2201
75177-010-10Hand Sanitizer300 mL in 1 BOTTLE, PLASTICLIQUID3001
75177-010-16Hand Sanitizer500 mL in 1 BOTTLE, PLASTICLIQUID5001
75177-010-33Hand Sanitizer1000 mL in 1 BOTTLE, PLASTICLIQUID10001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75177-010HAND SANITIZER (ALCOHOL) LIQUID [HERSTYLER, INC.]1Legacy NDC, 6 package rows20200414_a332169d-b73b-e25b-e053-2a95a90a60ea.zip

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75177-01075177-010-03, 75177-010-07, 75177-010-16, 75177-010-01, 75177-010-10, 75177-010-33

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 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
a3321c4e-1bce-f86f-e053-2995a90af49fa332169d-b73b-e25b-e053-2a95a90a60ea2020-04-13WarningsExact identifier
spl id: a3321c4e-1bce-f86f-e053-2995a90af49f
spl set id: a332169d-b73b-e25b-e053-2a95a90a60ea

Reported adverse events (FAERS/openFDA)#

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