Hand Sanitizer

Manufacturer
Uncle Jumbo’s Distillery,Inc | Uncle Jumbo’s Distillery Inc
Effective date
2020-05-01
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:09:17

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure12 sections

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

This is a hand sanitizer manufactured according to the Temporary Policy for Preparation of Certain Alcohol-Based Hand Sanitizer Products During the Public Health Emergency (CoViD-19); Guidance for Industry.

The hand sanitizer is manufactured using only the following United States Pharmacopoeia (USP) grade ingredients in the preparation of the product (percentage in final product formulation) consistent with World Health Organization (WHO) recommendations:

  1. Alcohol (ethanol) (USP or Food Chemical Codex (FCC) grade) (80%, volume/volume (v/v)) in an aqueous solution denatured according to Alcohol and Tobacco Tax and Trade Bureau regulations in 27 CFR part 20.
  2. Glycerol (1.45% v/v).
  3. Hydrogen peroxide (0.125% v/v).
  4. Sterile distilled water or boiled cold water.

The firm does not add other active or inactive ingredients. Different or additional ingredients may impact the quality and potency of the product.

Purpose

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer

Use

INDICATIONS & USAGE SECTION

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

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 80% v/v. Purpose: Antiseptic

Do not use

OTC - DO NOT USE SECTION

  • 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.
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.

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.

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.

OTC - STOP USE SECTION

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

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

250 ML front Label250 ML front Label250 ML Back Label250 ML Back Label250 mL NDC: 75526-000-00

354 ML Front Label354 ML Front Label354 ML Back Labe354 ML Back Labe354 ML 75526-000-02

3890 ML label3890 ML label

3890 ML 75526-000-01

175frnt175frnt175bk175bk1750ml 1.75 L front & Back

200mlbk200mlbk200mlfrnt200mlfrnt200 ml back & Frnt

473frnt473frnt473bk473bk473 ml Front & Back

946bck946bck946front946front946352 ml front & back

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1039339ethanol 80 % Topical SolutionPSN2
1039339ethanol 0.8 ML/ML Topical SolutionSCD2
1039339ethanol 80 % Topical SolutionSY2

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
75526-000-00Hand Sanitizer250 mL in 1 BOTTLE, PLASTICLIQUID2502
75526-000-01Hand Sanitizer3890 mL in 1 JUGLIQUID38902
75526-000-02Hand Sanitizer354 mL in 1 BOTTLE, PLASTICLIQUID3542
75526-000-03Hand Sanitizer200 mL in 1 BOTTLE, PLASTICLIQUID2002
75526-000-04Hand Sanitizer946352 mL in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULKLIQUID9463522
75526-000-05Hand Sanitizer473 mL in 1 BOTTLE, SPRAYLIQUID4732
75526-000-06Hand Sanitizer1750 mL in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULKLIQUID17502

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75526-000HAND SANITIZER (ISOPROPYL ALCOHOL) LIQUID [UNCLE JUMBO’S DISTILLERY,INC]2Legacy NDC, 7 package rows20200502_a360ab33-3f90-50e9-e053-2995a90acb96.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
75526-00075526-000-00, 75526-000-01, 75526-000-02, 75526-000-03, 75526-000-04, 75526-000-05, 75526-000-06

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
a4a06e2f-5775-4426-e053-2a95a90af603a360ab33-3f90-50e9-e053-2995a90acb962020-05-01WarningsExact identifier
spl id: a4a06e2f-5775-4426-e053-2a95a90af603
spl set id: a360ab33-3f90-50e9-e053-2995a90acb96

Reported adverse events (FAERS/openFDA)#

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