DEPENS PREMIUM SANITIZER

Manufacturer: HEALKINBIO CO.
Effective date: 2021-01-15
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:36:59

Label at a glance#

ProductDEPENS PREMIUM SANITIZER

Active ingredientalcohol

Label structure9 sections

Dosage and administration

 Take suitable amount of sanitizer in the hand. Wet thoroughly and rub hands together until dry

Storage and handling

 Store in room temperature 0~30℃  Period of Use: 36 Months after manufacturing date  Manufacturing Date and No. Printed on bottle

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethanol 70%

Purpose

OTC - PURPOSE SECTION

Purpose: Antiseptic

Use

INDICATIONS & USAGE SECTION

 Hand sanitizing to help reduce bacteria on the skin

Warnings

WARNINGS SECTION

 For external use only.
 Flammable, keep away from fire or flame.
 When using this product, avoid contact with the eyes. In case of contact, rinse eyes thoroughly with water.
 Stop use and ask a doctor if irritation or redness appears and lasts.

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 immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

 Take suitable amount of sanitizer in the hand. Wet thoroughly and rub hands together until dry

Other information

STORAGE AND HANDLING SECTION

 Store in room temperature 0~30℃

 Period of Use: 36 Months after manufacturing date

 Manufacturing Date and No. Printed on bottle

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water(Aqua), Carbomer, Triethanolamine, Polyoxyethylene Hydrogenated Caster Oil, Glycerin, Green Tea Extract, Aloe Extract, Tocopheryl Acetate, Fragrance(Parfum)

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
581662	ethanol 70 % Topical Gel	PSN	1
581662	ethanol 0.7 ML/ML Topical Gel	SCD	1
581662	ethanol 70 % Topical Gel	SY	1
581662	ethyl alcohol 70 % Topical Gel	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
76586-002-01	2023-01-30	C162847	48780-1	f386c64a-282a-0266-e053-dadaa90a7c1a	b22b547e-18c2-4d4b-9df9-85c79f5c0f80

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
76586-002-01	DEPENS PREMIUM SANITIZER	500 mL in 1 BOTTLE	Gel	500		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
76586-002	DEPENS PREMIUM SANITIZER (ADVANCED) GEL [HEALKINBIO CO.]	1	Legacy NDC, 1 package rows	20210116_b22b547e-18c2-4d4b-9df9-85c79f5c0f80.zip

Products#

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

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

DEPENS PREMIUM SANITIZER
ADVANCED
alcohol
Water
glycerin

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
76586-002	76586-002-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
alcohol	3K9958V90M	ACTIB
Water	059QF0KO0R	IACT
glycerin	PDC6A3C0OX	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
b0c5e5c8-af58-4310-b601-13ced39812e3			b22b547e-18c2-4d4b-9df9-85c79f5c0f80	2021-01-15	Warnings	Exact identifier spl id: b0c5e5c8-af58-4310-b601-13ced39812e3 spl set id: b22b547e-18c2-4d4b-9df9-85c79f5c0f80

Reported adverse events (FAERS/openFDA)#

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