Hand Sanitizer

Manufacturer
Spinster Sisters, Inc. | Spinster Sisters Inc.
Effective date
2021-10-26
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:44:30

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure11 sections

Indications and uses

Reduces bacteria on the skin

Dosage and administration

Shake well before using. Rub dime-sized amount all over both hands. Supervise children under 6. New version effective 4/2020: Shake well before using. Rub dime-sized amount all over both hands. Supervise children under 6. Previous version: Rub dime-sized amount on hands. Supervise children under 6.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 62%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

Reduces bacteria on the skin

Warnings

WARNINGS SECTION

  • For external use only.
  • Flammable. Keep away from fire and sparks. Do not store above 104°F/40°C.

Do not use

OTC - DO NOT USE SECTION

near eyes. In case of contact with eyes, rinse with water.

Stop use and ask a doctor

OTC - STOP USE SECTION

if skin irritation develops.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

Shake well before using. Rub dime-sized amount all over both hands. Supervise children under 6.

Directions

RECENT MAJOR CHANGES SECTION

New version effective 4/2020: Shake well before using. Rub dime-sized amount all over both hands. Supervise children under 6.

Previous version: Rub dime-sized amount on hands. Supervise children under 6.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Aloe Vera Gel [Aloe Barbadensis, Citric Acid, Sodium Benzoate, Potassium Sorbate, Sodium Sulfite], Mentha Piperita (Peppermint) Oil, Melaleuca Alternifolia (Tea Tree) Oil, and Glycerin

Questions?

OTC - QUESTIONS SECTION

Call 1-844-774-6783

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

73711-101-23 v173711-101-23 v173711-101-23 v273711-101-23 v273711-101-1973711-101-1973711-101-2973711-101-29

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
247835ethanol 62 % Topical SolutionPSN3
247835ethanol 0.62 ML/ML Topical SolutionSCD3
247835ethanol 62 % Topical SolutionSY3
247835ethyl alcohol 62 % Topical SolutionSY3

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73711-103-19Hand Sanitizer1900 mL in 1 BOTTLE, PLASTICLIQUID19003
73711-103-23Hand Sanitizer236 mL in 1 BOTTLE, PLASTICLIQUID2363
73711-103-29Hand Sanitizer29 mL in 1 BOTTLE, PLASTICLIQUID293

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73711-103HAND SANITIZER (ETHYL ALCOHOL) LIQUID [SPINSTER SISTERS, INC.]3Legacy NDC, 3 package rows20211028_a023b4cc-e9e7-df96-e053-2a95a90a3696.zip

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73711-10373711-103-29, 73711-103-19, 73711-103-23

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

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
cf44effe-aa8b-9bb7-e053-2a95a90adee4a023b4cc-e9e7-df96-e053-2a95a90a36962021-10-26WarningsExact identifier
spl id: cf44effe-aa8b-9bb7-e053-2a95a90adee4
spl set id: a023b4cc-e9e7-df96-e053-2a95a90a3696

Reported adverse events (FAERS/openFDA)#

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