Hand Sanitizer

Manufacturer
Biominerales Pharma
Effective date
2020-07-16
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:21:48

Label at a glance#

ProductHand Sanitizer
Active ingredientAlcohol
Label structure9 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

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

DRUG FACTS

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 80% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Inactive ingredients

INACTIVE INGREDIENT SECTION

Glycerin, Purified Water, Hydrogen Peroxide.

Use (s)

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria that potentially can cause disease. For use when water and soap 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 or on open skin wounds.

OTC - WHEN USING SECTION

When using this product keep our 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 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

SPL UNCLASSIFIED SECTION

Distributed by:
MPP Dist. LLC.
sales@mppint.com

PRINCIPAL DISPLAY PANEL - 3.785 L Container Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Alcohol Antiseptic 80% Topical Solution

MPP
INSTANT
HAND
SANITIZER

1 gallon
(3.785 L)

NDC: 77110-110-01

Distributed by:
MPP Dist. LLC.
sales@mppint.com

Kills 99.9% of Germs

PRINCIPAL DISPLAY PANEL - 3.785 L Container Label
PRINCIPAL DISPLAY PANEL - 3.785 L Container Label

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#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
77110-110-012022-01-28C16284748780-1d6a99b39-5cf5-a426-e053-dadaa90af4c2Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
77110-110-01Hand Sanitizer3785 mL in 1 CONTAINERSOLUTION37852

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
77110-110HAND SANITIZER (ALCOHOL) SOLUTION [BIOMINERALES PHARMA]2Legacy NDC, 1 package rows20200718_6cb243a5-bffa-46d8-b44b-c7002cd2116a.zip

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
77110-11077110-110-01

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
0cf8dfef-b3b7-46a8-b0f0-619ea97fc5ff6cb243a5-bffa-46d8-b44b-c7002cd2116a2020-07-16WarningsExact identifier
spl id: 0cf8dfef-b3b7-46a8-b0f0-619ea97fc5ff
spl set id: 6cb243a5-bffa-46d8-b44b-c7002cd2116a

Reported adverse events (FAERS/openFDA)#

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