Dr. Bancrofts Hand Sanitizer

Manufacturer: Sazerac Company, Inc.
Effective date: 2020-06-06
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: legacy-cache
Hydrated at: 2026-08-01 23:27:23

Label at a glance#

ProductDr. Bancrofts 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 80% 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 • in 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

glycerin, hydrogen peroxide, purified water USP

Package Label - 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 80%

TOPICAL SOLUTION

NON-STERILE

3.4 FL OZ (100 mL)

MANUFACTURED BY SAZERAC COMPANY • 10101 LINN STATION ROAD

LOUISVILLE, KY 40233

Dr B 100 mL

200 mL

Dr B 200 mL

375 mL

Dr B 375 mL

1.75 L

Dr B 1.75 L

res

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
75089-200-01	2022-12-28	C162847	48780-1	d6a99b39-7409-a426-e053-dadaa90af4c2	3d51feb8-2e90-416b-a4ae-8f6d2048ec7d
75089-200-02	2022-12-28	C162847	48780-1	d6a99b39-7409-a426-e053-dadaa90af4c2	3d51feb8-2e90-416b-a4ae-8f6d2048ec7d
75089-200-03	2022-12-28	C162847	48780-1	d6a99b39-7409-a426-e053-dadaa90af4c2	3d51feb8-2e90-416b-a4ae-8f6d2048ec7d
75089-200-04	2022-12-28	C162847	48780-1	d6a99b39-7409-a426-e053-dadaa90af4c2	3d51feb8-2e90-416b-a4ae-8f6d2048ec7d
75089-200-01	2022-01-28	C162847	48780-1	d6a99b39-7409-a426-e053-dadaa90af4c2	3d51feb8-2e90-416b-a4ae-8f6d2048ec7d
75089-200-02	2022-01-28	C162847	48780-1	d6a99b39-7409-a426-e053-dadaa90af4c2	3d51feb8-2e90-416b-a4ae-8f6d2048ec7d
75089-200-03	2022-01-28	C162847	48780-1	d6a99b39-7409-a426-e053-dadaa90af4c2	3d51feb8-2e90-416b-a4ae-8f6d2048ec7d
75089-200-04	2022-01-28	C162847	48780-1	d6a99b39-7409-a426-e053-dadaa90af4c2	3d51feb8-2e90-416b-a4ae-8f6d2048ec7d

Products#

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

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

Dr. Bancrofts Hand Sanitizer
Alcohol
GLYCERIN
HYDROGEN PEROXIDE
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
75089-200	75089-200-01, 75089-200-02, 75089-200-03, 75089-200-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ALCOHOL	3K9958V90M	ACTIB
GLYCERIN	PDC6A3C0OX	IACT
HYDROGEN PEROXIDE	BBX060AN9V	IACT
WATER	059QF0KO0R	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
6d810ca5-ae08-4f0f-a084-d15cd9c480f9			3d51feb8-2e90-416b-a4ae-8f6d2048ec7d	2022-12-28	Warnings	Exact identifier spl set id: 3d51feb8-2e90-416b-a4ae-8f6d2048ec7d

Reported adverse events (FAERS/openFDA)#

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