FDA.reportPublic FDA data

Andys

Manufacturer
Brand Name Distributors LLC
Effective date
2020-04-23
Label type
HUMAN OTC DRUG LABEL
Version
7
Source
legacy-cache
Hydrated at
2026-08-01 23:34:37

Label at a glance#

ProductAndys
Active ingredientALCOHOL
Label structure9 sections

Dosage and administration

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

Label contents#

Full prescribing information#

DRUG FACTS

OTC - ACTIVE INGREDIENT SECTION

ACTIVE INGREDIENTS .............................PURPOSE

ETHYL ALCOHOL 70%..............................ANTIMICROBIAL

ACTIVE INACTIVE IN

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

CARBOMER, TRIETHANOLAMINE LAURYL SULFATE, WATER

INACTIVEINACTIVE

Directions

DOSAGE & ADMINISTRATION SECTION


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

DirectionsDirections

WARNING SECTION

WARNINGS SECTION

Flammable. Keep away from fire or flame. For external use only. When using this product:

Don't use in or near the eyes. In the case of contact, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation or rash appears and lasts.

WarningWarning

Keep out of reach of children section

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children section

keepkeep

USE

OTC - PURPOSE SECTION

Hand Sanitizer to help reduce bacteria on the skin

USEUSE

USE and Indications

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria on the skin

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

use2use2

HAND SANITIZER UNSCENTED

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

HAND SANITIZER UNSCENTED

Kills Over 99% of Most
Common Germs

Refill your bottle of Hand Sanitizer in

* Kitchen * Automobile * Offices* Bathrooms *

Size conversion: For the point of reference each container jug contains 692 fluid oz. and is the equivalent of roughly 346 - 2oz. bottles or 87 - 8oz. bottles making our bulk container sizes a great value.

*FOR PERSONAL REFILL USE ONLY

676.28 FL OZ (20L)

IMAGE FRONTIMAGE FRONT

.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Hand Sanitizer frofro

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
73755-13073755-130-02

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
TRIETHANOLAMINE LAURYL SULFATEE8458C1KAAIACT
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
CARBOMER 1342809Y72KV36IACT

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
aaaaaa25-21c4-3974-e053-2a95a90a46dea17aa834-afc3-7ce6-e053-2a95a90ac4a32020-07-17WarningsExact identifier
spl set id: a17aa834-afc3-7ce6-e053-2a95a90ac4a3

Reported adverse events (FAERS/openFDA)#

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