Hand Sanitizer

Manufacturer
Hopkins Medical | Safetec of America, Inc.
Effective date
2020-03-23
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:04:13

Label at a glance#

ProductHand Sanitizer
Active ingredientalcohol
Label structure7 sections

Indications and uses

for handwashing to decrease bacteria on skin recommended for repeated use

Dosage and administration

wet hands thoroughly with product allow to dry without wiping children under 6 should be supervised while using this product

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 66.5%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

  • for handwashing to decrease bacteria on skin
  • recommended for repeated use

Warnings

WARNINGS SECTION

SPL UNCLASSIFIED SECTION

For external use only

Flammable, keep away from fire or flame

OTC - DO NOT USE SECTION

Do not use in the eyes. If this happens, rinse thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation and redness develop and persists for more than 72 hours

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If ingested get medical help or contact a Poison Control Center right away

Directions

DOSAGE & ADMINISTRATION SECTION

  • wet hands thoroughly with product
  • allow to dry without wiping
  • children under 6 should be supervised while using this product

Inactive ingredients

INACTIVE INGREDIENT SECTION

aloe vera, carbomer, D&C green #5, D&C yellow #10, fragrance, purified water, triethanolamine

Principal Display Panel – 1.5 fl. oz. Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Hopkins
Waterless
Hand
Sanitizer

Enriched with Aloe

Hopkins

Medical Products

Since 1945

1.5 FL OZ (46 ML)

#697373

Principal Display Panel – 1.5 fl. oz. Bottle Label
Principal Display Panel – 1.5 fl. oz. Bottle Label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
44662-1112-02022-01-28C16284748780-1d6a99b39-885c-a426-e053-dadaa90af4c2Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
44662-1112-0Hand Sanitizer0.046 L in 1 BOTTLEGEL0.0461

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
44662-1112HAND SANITIZER (ALCOHOL) GEL [HOPKINS MEDICAL]1Legacy NDC, 1 package rows20200327_d818ad25-0fc4-441d-82e5-38374bee6c22.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
44662-111244662-1112-0

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 · Source PDF

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
4810b30b-d27f-4051-92d1-1cd3d53c9fefd818ad25-0fc4-441d-82e5-38374bee6c222020-03-23WarningsExact identifier
spl id: 4810b30b-d27f-4051-92d1-1cd3d53c9fef
spl set id: d818ad25-0fc4-441d-82e5-38374bee6c22

Reported adverse events (FAERS/openFDA)#

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