LUSTI Skin Softening hand sanitizer

Manufacturer: New Life Products, Inc.
Effective date: 2023-02-02
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: full-release
Hydrated at: 2026-05-31 23:53:41

Label at a glance#

ProductLUSTI Skin Softening hand sanitizer

Active ingredientALCOHOL

Label structure8 sections

Contacts and useful links#

Websitewww.afamconcept.com

www.afamconcept.com

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 65%

Purpose

OTC - PURPOSE SECTION

Antiseptic

INDICATIONS & USAGE SECTION

Use • Hand sanitizer to decrease bacteria on skin • Recommended for repeated use

WARNINGS SECTION

Warnings • For external use only. Flammable.

Keep away from fire or flame.

When using this product avoid contact with face, eyes and broken skin. If eye contact occurs, flush thoroughly with water and seek medical advice.

Stop use and ask a doctor if irritation and redness develops.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

DOSAGE & ADMINISTRATION SECTION

Directions• Wet hands thoroughly with product and rub into skin until dry.

• Children under 6 years of age should be supervised by an adult when using this product

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Isopropyl Alcohol, Glycerin, Carbomer, Aminomethyl Propanol, Mentha Piperita (Peppermint) Oil, Panthenol, Tocopheryl Acetate, Fragrance(Parfum).

SPL UNCLASSIFIED SECTION

ADVANCED FORMULA

with PEPPERMINT OIL

KILLS GERMS FAST &

LEAVES HANDS SOFT & PROTECTED

JF LABS INC. Chicago,IL 60629

(800)262-2326 Watford WD247GN, UK

www.afamconcept.com ISO and cGMP compliant

MADE IN USA

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Packaging

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
884783	ethanol 65 % Topical Solution	PSN	3
884783	ethanol 0.65 ML/ML Topical Solution	SCD	3
884783	ethanol 65 % Topical Solution	SY	3

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
49681-400-04	2024-07-30	C162847	48780-1	f386c64a-3928-0266-e053-dadaa90a7c1a	Lusti ® SKIN SOFTENING HAND SANITIZER
49681-400-04	2024-01-30	C162847	48780-1	f386c64a-3928-0266-e053-dadaa90a7c1a	Lusti ® SKIN SOFTENING HAND SANITIZER
49681-400-04	2023-02-02	C162847	48780-1	f386c64a-3928-0266-e053-dadaa90a7c1a	Lusti ® SKIN SOFTENING HAND SANITIZER
49681-400-04	2023-01-30	C162847	48780-1	f386c64a-3928-0266-e053-dadaa90a7c1a	Lusti ® SKIN SOFTENING HAND SANITIZER

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
49681-400-04	LUSTI Skin Softening hand sanitizer	118 mL in 1 BOTTLE	LIQUID	118		3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
49681-400	LUSTI SKIN SOFTENING HAND SANITIZER (ETHYL ALCOHOL) LIQUID [NEW LIFE PRODUCTS, INC.]	3	Legacy NDC, 1 package rows	20230203_b91bedd3-b672-440a-abae-98462361b486.zip

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

LUSTI Skin Softening hand sanitizer
Ethyl Alcohol
ALCOHOL
WATER
ISOPROPYL ALCOHOL
GLYCERIN
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE
AMINOMETHYLPROPANOL
PEPPERMINT OIL
PANTHENOL
.ALPHA.-TOCOPHEROL ACETATE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
49681-400	49681-400-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ALCOHOL	3K9958V90M	ACTIB
WATER	059QF0KO0R	IACT
ISOPROPYL ALCOHOL	ND2M416302	IACT
GLYCERIN	PDC6A3C0OX	IACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE	0A5MM307FC	IACT
AMINOMETHYLPROPANOL	LU49E6626Q	IACT
PEPPERMINT OIL	AV092KU4JH	IACT
PANTHENOL	WV9CM0O67Z	IACT
.ALPHA.-TOCOPHEROL ACETATE	9E8X80D2L0	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 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
4f00c0ed-885d-418e-aef8-ed000d1d6f5c			b91bedd3-b672-440a-abae-98462361b486	2023-02-02	Warnings	Exact identifier spl id: 4f00c0ed-885d-418e-aef8-ed000d1d6f5c spl set id: b91bedd3-b672-440a-abae-98462361b486

Reported adverse events (FAERS/openFDA)#

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