FDA.reportPublic FDA data

Andys Best

Manufacturer
Brand Name Distributor | Limpo Químicos, S.A. de C.V.
Effective date
2020-05-17
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:30:27

Label at a glance#

ProductAndys Best
Active ingredientALCOHOL
Label structure13 sections

Dosage and administration

Put a enough product in your palm to cover hands and rub hands together briskly until dry Children under 6 years of age should be supervised when using Andys

Storage and handling

Store below 110 F(43 C) May discolor certain fabrics of surfaces

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 70% v/v. Purpose: Antimicrobial

Active IngredientActive Ingredient

Purpose

OTC - PURPOSE SECTION

Antimicrobial, Hand Sanitizer

PurposePurpose

Use

INDICATIONS & USAGE SECTION

IndicationIndicationHand 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

WarningWarning

Do not use

OTC - DO NOT USE SECTION

  • Do not useDo not usein 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.

when usewhen use

OTC - STOP USE SECTION

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

Stop UseStop Use

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.

keep outkeep out

Directions

DOSAGE & ADMINISTRATION SECTION

Put a enough product in your palm to cover hands and rub hands together briskly until dry

Children under 6 years of age should be supervised when using Andys

DosageDosage

Other information

STORAGE AND HANDLING SECTION

Store below 110 F(43 C)

May discolor certain fabrics of surfaces

StorageStorage

Inactive ingredients

INACTIVE INGREDIENT SECTION

Carbomer, triethanollamine lauryl sulfate, water InactiveInactive

RECENT MAJOR CHANGES SECTION

Major changesMajor changes

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Advanced Hand Sanitizer - Unscented Kills Over 99% of most common germs

1 gallon , 128 OZ , 3.8L

FrontFront

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73755-120-012024-01-30C16284748780-11030e365-5ac6-111a-e063-dadaa90a10e2a36008c5-7f4f-0c55-e053-2a95a90a5592
73755-120-022024-01-30C16284748780-11030e365-5ac6-111a-e063-dadaa90a10e2a36008c5-7f4f-0c55-e053-2a95a90a5592

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
73755-12073755-120-01, 73755-120-02

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
NameUNIIKind
CARBOMER 934Z135WT9208IACT
TRIETHANOLAMINE LAURYL SULFATEE8458C1KAAIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB

Source Document#

Source XML · Source PDF

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
aaaaac25-b0d2-3904-e053-2a95a90a4bdaa36008c5-7f4f-0c55-e053-2a95a90a55922020-07-17WarningsExact identifier
spl set id: a36008c5-7f4f-0c55-e053-2a95a90a5592

Reported adverse events (FAERS/openFDA)#

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