Andys

Manufacturer: Brand Name Distributors
Effective date: 2020-03-29
Label type: HUMAN OTC DRUG LABEL
Version: 4
Source: full-release
Hydrated at: 2026-05-31 23:04:16

Label at a glance#

ProductAndys

Active ingredientALCOHOL

Label structure8 sections

Dosage and administration

USE Hand Sanitizer to help reduce bacteria on the skin INDICATION Put enough product in your palm to cover hands and rub hands together briskly until dry

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% .........................Antimicrobial

ACTIVE

DIRECTIONS AND USD

INDICATIONS & USAGE SECTION

USE Hand Sanitizer to help reduce bacteria on the skin

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

USE

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Carbomer, Triethanolamine Lauryl Sulfate, water

Inactive

WARNING

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.

warning

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 poison control center right away

KEEP

PURPOSE

OTC - PURPOSE SECTION

Antimicrobial

Anti

DOSAGE

DOSAGE & ADMINISTRATION SECTION

USE Hand Sanitizer to help reduce bacteria on the skin

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

DOSAGE

ANDY's HAND SANITIZER Unscented

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Kills Over 99% of Most Common Germs

Refill your bottle of Hand Sanitizer in

* Kitchen * Automobile * Offices* Bathrooms *

125.11 FL OZ (3.7L)

Front

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
581662	ethanol 70 % Topical Gel	PSN	4
581662	ethanol 0.7 ML/ML Topical Gel	SCD	4
581662	ethanol 70 % Topical Gel	SY	4
581662	ethyl alcohol 70 % Topical Gel	SY	4

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
73755-110-01	2021-07-23	C162847	48780-1	c7ccaba7-0f30-fd44-e053-dadaa90aa01b	a0dfa284-81b7-f299-e053-2995a90aef7d

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
73755-110-01	Andys	3785 mL in 1 BOTTLE	GEL	3785		4

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
73755-110	ANDYS (ALCOHOL) GEL [BRAND NAME DISTRIBUTORS]	4	Legacy NDC, 1 package rows	20200330_a0dfa284-81b7-f299-e053-2995a90aef7d.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

Andys
ALCOHOL
WATER O-18
TROLAMINE
CARBOMER 1342

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
73755-110	73755-110-01

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
Name	UNII	Kind
ALCOHOL	3K9958V90M	ACTIB
WATER O-18	7QV8F8BYNJ	IACT
TROLAMINE	9O3K93S3TK	IACT
CARBOMER 1342	809Y72KV36	IACT

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
a20280c5-15b4-89b9-e053-2a95a90afb04			a0dfa284-81b7-f299-e053-2995a90aef7d	2020-03-29	Warnings	Exact identifier spl id: a20280c5-15b4-89b9-e053-2a95a90afb04 spl set id: a0dfa284-81b7-f299-e053-2995a90aef7d

Reported adverse events (FAERS/openFDA)#

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