Dr. Bancrofts Gel Hand Sanitizer

Manufacturer
Sazerac Company, Inc.
Effective date
2020-07-21
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:20:29

Label at a glance#

ProductDr. Bancrofts Gel Hand Sanitizer
Active ingredientALCOHOL
Label structure13 sections

Dosage and administration

Place enough product on hands to cover all surfaces. Rub hands together until dry.  Supervise children under 6 years of age when using this product to avoid swallowing.

Storage and handling

Store between 15-30C (59-86F) Avoid freezing and excessive heat above 40C (104F)

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient([s]

Denatured Alcohol 70% v/v

OTC - PURPOSE SECTION

Purpose

Antiseptic

INDICATIONS & USAGE SECTION

Use[s]  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 heat or flame

OTC - DO NOT USE SECTION

Do not use  • on children less than 2 months of age • on open skin wounds

OTC - WHEN USING SECTION

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

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

  • Place enough product on hands to cover all surfaces. Rub hands together until dry.  Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

STORAGE AND HANDLING SECTION

  • Store between 15-30C (59-86F)
  • Avoid freezing and excessive heat above 40C (104F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

aminomethylpropanol, carbomer, purified water

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

FREE OF FRAGRANCES AND DYES

Dr. Bancroft's

HAND
SANITIZER

PROUDLY MADE IN THE U.S.A.

ALCOHOL ANTISEPTIC 70%
TOPICAL SOLUTION
NON-STERILE SOLUTION

3.4 FL OZ (100 mL)

MANUFACTURED BY SAZERAC COMPANY • 10101 LINN STATION ROAD
LOUISVILLE, KY 40223 • QUESTIONS? 866-729-3722

75089_301_0575089_301_05

res

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
75089-301-052022-12-28C16284748780-1d6a99b39-de63-a426-e053-dadaa90af4c2DR. BANCROFT'S GEL HAND SANITIZER
75089-301-052022-01-28C16284748780-1d6a99b39-de63-a426-e053-dadaa90af4c2DR. BANCROFT'S GEL HAND SANITIZER

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75089-30175089-301-05

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 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
076a1cb7-d7b2-45d1-949b-500ca9dc625d3016c084-1bd3-40b1-8050-f38d80ec62112022-12-28WarningsExact identifier
spl set id: 3016c084-1bd3-40b1-8050-f38d80ec6211

Reported adverse events (FAERS/openFDA)#

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