Backdrop Distilling Hand Sanitizer

Manufacturer
Backdrop Distilling
Effective date
2020-03-31
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:04:54

Label at a glance#

ProductBackdrop Distilling Hand Sanitizer
Active ingredientALCOHOL
Label structure14 sections

Indications and uses

Use(s) Hand Sanitizer to help reduce bacteria that potentially cause disease. For use when soap and water are not available. Directions -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.

Dosage and administration

Directions -Place enough product on the hands to cover all surfaces. 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 and Back Label

OTC - ACTIVE INGREDIENT SECTION

Drug FactsDrug FactsEthyl Alcohol 70% v/v Purpose Antiseptic

Do not use

OTC - DO NOT USE SECTION

Do not use

-in children less than 2 months of age

-on open skin wounds

Keep out of reach of children

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.

Purpose section

OTC - PURPOSE SECTION

Use(s)

Hand Sanitizer to help reduce bacteria that potentially

can casue disease. For use when soap and water are not

available.

Stop use section

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash occurs.

These may be signs of a serious condition.

When using

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.

Other safety

OTHER SAFETY INFORMATION

Other information

-Store between 15-30C (59-86F)

-Avoid freezing and excessive heat above 40C (104F)

Warnings

WARNINGS AND PRECAUTIONS SECTION

Warnings

For external use only. Flammable. Keep away from

heat or flame.

Directions

INSTRUCTIONS FOR USE SECTION

Directions

-Place enough product on the hands to cover all surfaces.

Rub hands together until dry.

-Supervise children under 6 years of age when using

this product to avoid swallowing.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Inactive ingredients glycerin, hydrogen

peroxide, purified water

Dosage

DOSAGE & ADMINISTRATION SECTION

Directions

-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.

Warnings

WARNINGS SECTION

Warnings

For external use only. Flammable. Keep away from

heat or flame.

Do not use

-In children less than 2 months of age

-on open skin wounds

When using this product keep out of eyes, ears, and

mouth. In case of contact with eyes, rinse eyes

thoroughly with water.

Stop use and ask a doctor if irritation or rash occurs.

These may be signs of a serious condition.

Keep out of reach of children. If swallowed, get

medical help or contact a Poison Control Center right

away.

Indications and usage

INDICATIONS & USAGE SECTION

Use(s)

Hand Sanitizer to help reduce bacteria that potentially

cause disease. For use when soap and water are not

available.

Directions

-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.

Front Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Front LabelFront Label(Logo)

Hand Sanitizer

Alcohol Antiseptic 70%

Topical Solution Hand Santizer

Non-sterile Solution

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
5eb9f24b-9328-475e-af0a-18021935eb6aProduct name120180220

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74289-001-01Backdrop Distilling Hand Sanitizer946.35 mL in 1 BOTTLE, PLASTICLIQUID946.351
74289-001-02Backdrop Distilling Hand Sanitizer3785.41 mL in 1 BOTTLE, PLASTICLIQUID3785.411
74289-001-03Backdrop Distilling Hand Sanitizer473.176 mL in 1 BOTTLE, PLASTICLIQUID473.1761
74289-001-04Backdrop Distilling Hand Sanitizer59.147 mL in 1 BOTTLE, SPRAYLIQUID59.1471

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74289-001BACKDROP DISTILLING HAND SANITIZER (BACKDROP HAND SANITIZER ETHENOL) LIQUID [BACKDROP DISTILLING]1Legacy NDC, 4 package rows20200404_a22d4aae-76c9-75c1-e053-2a95a90aad81.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74289-00174289-001-01, 74289-001-02, 74289-001-03, 74289-001-04

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
a22d4aae-76ca-75c1-e053-2a95a90aad81a22d4aae-76c9-75c1-e053-2a95a90aad812020-03-31WarningsExact identifier
spl id: a22d4aae-76ca-75c1-e053-2a95a90aad81
spl set id: a22d4aae-76c9-75c1-e053-2a95a90aad81

Reported adverse events (FAERS/openFDA)#

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