Antiseptic

Manufacturer: Welly Health PCB
Effective date: 2019-11-05
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-05-31 23:03:39

Label at a glance#

ProductAntiseptic

Active ingredientalcohol

Label structure8 sections

Indications and uses

For handwashing to decrease bacteria on skin without soap and water Recommended for repeated use

Dosage and administration

Wet hands & wrists thoroughly with product and allow to dry without wiping Children under 6 years of age should be supervised while using this product

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 66.5%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

For handwashing to decrease bacteria on skin without soap and water
Recommended for repeated use

Warnings

WARNINGS SECTION

SPL UNCLASSIFIED SECTION

For external use only.

Flammable, keep away from fire or flame.

OTC - DO NOT USE SECTION

Do not use in eyes. If this happens, rinse thoroughly with water

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation and redness develop and persists for more than 72 hours

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep this and all drugs out of the reach of children. If ingested get medical help or contact a Poison Control Center right away

Directions

DOSAGE & ADMINISTRATION SECTION

Wet hands & wrists thoroughly with product and allow to dry without wiping
Children under 6 years of age should be supervised while using this product

Inactive Ingredients

INACTIVE INGREDIENT SECTION

aloe vera, carbomer, D&C green #5, D&C yellow #10, fragrance, purified water, triethanolamine

Principal Display Panel – Box Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

OINTMENT REFILLS

Welly FIRST AID

Clean Hands
INSTANT HAND SANITIZER

COUNT 12

NET WT 0.03 oz (0.9g)

TOTAL NET WT 0.36 oz (10.8g)

Ethyl Alcohol

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
616762	ethanol 66.5 % Topical Gel	PSN	2
616762	ethanol 0.665 ML/ML Topical Gel	SCD	2
616762	ethanol 66.5 % Topical Gel	SY	2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
72663-111-12	Antiseptic	12 in 1 BOX	GEL	12		2
72663-111-23	Antiseptic	0.9 mL in 1 POUCH	GEL	0.9		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
72663-111	ANTISEPTIC (ALCOHOL) GEL [WELLY HEALTH PCB]	2	Current NDC, Legacy NDC, 2 package rows	20200207_515a2c1d-2c2c-4389-b042-0e880661db64.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

Antiseptic
alcohol
aloe vera leaf
carbomer interpolymer type a (allyl sucrose crosslinked)
D&C green no. 5
D&C yellow no. 10
water
trolamine

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
72663-111	72663-111-23, 72663-111-12

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
alcohol	3K9958V90M	ACTIB
aloe vera leaf	ZY81Z83H0X	IACT
carbomer interpolymer type a (allyl sucrose crosslinked)	59TL3WG5CO	IACT
D&C green no. 5	8J6RDU8L9X	IACT
D&C yellow no. 10	35SW5USQ3G	IACT
water	059QF0KO0R	IACT
trolamine	9O3K93S3TK	IACT

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 · 2 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Antiseptic	ALCOHOL	Welly Health PCB	85ce2c23-25d8-4b35-95ff-99f098d92bc9	2025-01-29	Warnings	Exact identifier ndc (package): 72663-111-23 ndc (product): 72663-111 ndc11 (package): 72663011123
ccaa8a68-c8f9-40ea-b075-187216a4fdd5			515a2c1d-2c2c-4389-b042-0e880661db64	2019-11-05	Warnings	Exact identifier spl id: ccaa8a68-c8f9-40ea-b075-187216a4fdd5 spl set id: 515a2c1d-2c2c-4389-b042-0e880661db64

Reported adverse events (FAERS/openFDA)#

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