SeaLuxe Hand Sanitizer

Manufacturer: APR Beauty Group Inc.
Effective date: 2020-08-31
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: full-release
Hydrated at: 2026-05-31 23:28:45

Label at a glance#

ProductSeaLuxe Hand Sanitizer

Active ingredientALCOHOL

Label structure9 sections

Indications and uses

Kills harmful bacteria/germs

Dosage and administration

Rub thoroughly into hands for at least 30 seconds until dry. For children 2 years and over supervise when product is used

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol, 70% w/w

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

Kills harmful bacteria/germs

Warnings

WARNINGS SECTION

Flammable, keep away from open flame and sources of heat.

OTC - WHEN USING SECTION

For occasional and personal domestic use.

OTC - STOP USE SECTION

Stop use and consult a health care practitioner if irritation develops.

Avoid contact with eyes.

If contact occurs, rinse thoroughly with water.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, call a posion control centre.

Directions

DOSAGE & ADMINISTRATION SECTION

Rub thoroughly into hands for at least 30 seconds until dry.

For children 2 years and over supervise when product is used

Other Information

SPL UNCLASSIFIED SECTION

Recommended storage conditions:

20 Degress Celsius

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Aloe barbadensis leaf juice, Aminomethyl Propanol, Glycerin , Propylene Glycol, Water, Isopropyl Myristate,Carbomer

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

123

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
581662	ethanol 70 % Topical Gel	PSN	3
581662	ethanol 0.7 ML/ML Topical Gel	SCD	3
581662	ethanol 70 % Topical Gel	SY	3
581662	ethyl alcohol 70 % Topical Gel	SY	3

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
79959-001-24	2022-01-28	C162847	48780-1	d6a99b39-614d-a426-e053-dadaa90af4c2	Naturaluxe Hand Sanitizer
79959-001-35	2022-01-28	C162847	48780-1	d6a99b39-614d-a426-e053-dadaa90af4c2	Naturaluxe Hand Sanitizer
79959-001-50	2022-01-28	C162847	48780-1	d6a99b39-614d-a426-e053-dadaa90af4c2	Naturaluxe Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
79959-001-24	SeaLuxe Hand Sanitizer	240 mL in 1 BOTTLE	GEL	240	3
79959-001-35	SeaLuxe Hand Sanitizer	315 mL in 1 BOTTLE	GEL	315	3
79959-001-50	SeaLuxe Hand Sanitizer	500 mL in 1 BOTTLE	GEL	500	3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
79959-001	SEALUXE HAND SANITIZER (ETHYL ALCOHOL) GEL [APR BEAUTY GROUP INC.]	3	Legacy NDC, 3 package rows	20200909_ac7d5dcb-54bf-43ba-a56b-52969c89ccac.zip

Products#

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

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

SeaLuxe Hand Sanitizer
Ethyl Alcohol
ISOPROPYL MYRISTATE
WATER
PROPYLENE GLYCOL
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)
GLYCERIN
ALOE VERA LEAF
AMINOMETHYLPROPANOL
TOCOPHEROL
ALCOHOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
79959-001	79959-001-24, 79959-001-50, 79959-001-35

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
ISOPROPYL MYRISTATE	0RE8K4LNJS	IACT
WATER	059QF0KO0R	IACT
PROPYLENE GLYCOL	6DC9Q167V3	IACT
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)	59TL3WG5CO	IACT
GLYCERIN	PDC6A3C0OX	IACT
ALOE VERA LEAF	ZY81Z83H0X	IACT
AMINOMETHYLPROPANOL	LU49E6626Q	IACT
TOCOPHEROL	R0ZB2556P8	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
ae2d7bff-6daf-61e0-e053-2a95a90a3216			ac7d5dcb-54bf-43ba-a56b-52969c89ccac	2020-08-31	Warnings	Exact identifier spl id: ae2d7bff-6daf-61e0-e053-2a95a90a3216 spl set id: ac7d5dcb-54bf-43ba-a56b-52969c89ccac

Reported adverse events (FAERS/openFDA)#

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