KLENLII SUBWAY ALCOHOL SANITIZER GEL (62% ETHYL ALCOHOL) (78016-103)

Manufacturer: Klenlii Company
Effective date: 2024-05-09
Label type: HUMAN OTC DRUG LABEL
Version: 4
Source: full-release
Hydrated at: 2026-06-01 00:12:20

Label at a glance#

ProductSUBWAY ALCOHOL SANITIZER

Active ingredientALCOHOL

Label structure8 sections

Indications and uses

DECREASE BACTERIA ON SKIN THAT COULD CAUSE DISEASE RECOMMENDED FOR REPEATED USE

Dosage and administration

WET HANDS THOROUGHLY WITH PRODUCT AND ALLOW TO DRY WITHOUT WIPING NOT FOR CHILDREN UNDER 6, USE ONLY UNDER ADULT SUPERVISION NOT RECOMMENDED FOR INFANTS

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

ETHYL ALCOHOL 62%

PURPOSE

OTC - PURPOSE SECTION

ANTISEPTIC

USES

INDICATIONS & USAGE SECTION

DECREASE BACTERIA ON SKIN THAT COULD CAUSE DISEASE
RECOMMENDED FOR REPEATED USE

WARNINGS

WARNINGS SECTION

FOR EXTERNAL USE ONLY: HANDS

FLAMMABLE, KEEP AWAY FROM FIRE OR FLAME.

WHEN USING THIS PRODUCT

KEEP OUT OF EYES
IN CASE OF CONTACT WITH EYES, FLUSH THOROUGHLY WITH WATER
AVOID CONTACT WITH BROKEN SKIN
DO NOT INHALE OR DIGEST

STOP USE AND ASK DOCTOR IF

IRRITATION OR REDNESS DEVELOPS
CONDITION PERSISTS MORE THAN 72 HOURS

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.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

WET HANDS THOROUGHLY WITH PRODUCT AND ALLOW TO DRY WITHOUT WIPING
NOT FOR CHILDREN UNDER 6, USE ONLY UNDER ADULT SUPERVISION
NOT RECOMMENDED FOR INFANTS

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

DEIONIZED WATER, CARBOPOL, GLYCERIN, FRAGRANCE

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

01b LBL_klenlii_Subway

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
581660	ethanol 62 % Topical Gel	PSN	4
581660	ethanol 0.62 ML/ML Topical Gel	SCD	4
581660	ethanol 62 % Topical Gel	SY	4

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
78016-103-16	2024-05-09	C162847	48780-1	1030e365-5c2b-111a-e063-dadaa90a10e2	KLENLII SUBWAY ALCOHOL SANITIZER GEL (62% ETHYL ALCOHOL) (78016-103)
78016-103-16	2024-01-30	C162847	48780-1	1030e365-5c2b-111a-e063-dadaa90a10e2	KLENLII SUBWAY ALCOHOL SANITIZER GEL (62% ETHYL ALCOHOL) (78016-103)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
78016-103-16	SUBWAY ALCOHOL SANITIZER	473 mL in 1 BOTTLE	GEL	473		4

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
78016-103	SUBWAY ALCOHOL SANITIZER (ETHYL ALCOHOL) GEL [KLENLII COMPANY]	4	Legacy NDC, 1 package rows	20240511_45794deb-194c-4473-8e1c-811244663509.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

SUBWAY ALCOHOL SANITIZER
ETHYL ALCOHOL
WATER
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE
GLYCERIN
ALCOHOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
78016-103	78016-103-16

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
WATER	059QF0KO0R	IACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE	0A5MM307FC	IACT
GLYCERIN	PDC6A3C0OX	IACT
ALCOHOL	3K9958V90M	ACTIB

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
180c54a7-0723-0e04-e063-6394a90a8b54			45794deb-194c-4473-8e1c-811244663509	2024-05-09	Warnings	Exact identifier spl id: 180c54a7-0723-0e04-e063-6394a90a8b54 spl set id: 45794deb-194c-4473-8e1c-811244663509

Reported adverse events (FAERS/openFDA)#

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