Dr. Dris Hand Sanitizer

Manufacturer: Hanson Venture Enterprise Inc. | Natures Formulae Health Products Ltd.
Effective date: 2021-01-13
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:36:52

Label at a glance#

ProductDr. Dris Hand Sanitizer

Active ingredientALCOHOL

Label structure13 sections

Indications and uses

Hand sanitizer to help reduce bacteria on the skin. For use when soap and water are not available.

Dosage and administration

• place enough product on hands to cover all surfaces. Rub hands together until dry • supervise children under 6 years of age when using this product to avoid swallowing

Storage and handling

• store in a cool dry place. Do not overheat.

Contacts and useful links#

PhoneLabel contact1-213-235-8072

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 68% v/v

Purpose

OTC - PURPOSE SECTION

Ethyl Alcohol 68% v/v................Antiseptic

Uses

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria on the skin.
For use when soap and water are not available.

Warnings

WARNINGS SECTION

For external use only.

Flammable. Keep away from heat or flame.

OTC - DO NOT USE SECTION

Do not use:

• on children less than 2 months of age
• on open skin wounds

OTC - WHEN USING SECTION

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of the reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

• place enough product on hands to cover all surfaces. Rub hands together until dry
• supervise children under 6 years of age when using this product to avoid swallowing

Other Information

STORAGE AND HANDLING SECTION

• store in a cool dry place. Do not overheat.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Purified Water, Aloe Vera Leaf Juice, Hydroxyethyl Cellulose, Peppermint Oil

Questions or Comments?

SPL UNCLASSIFIED SECTION

Call 1-213-235-8072 Monday through Friday, 1pm-5pm PST

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PDP

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
2286291	ethanol 68 % Topical Solution	PSN	1
2286291	ethanol 0.68 ML/ML Topical Solution	SCD	1
2286291	ethanol 68 % Topical Solution	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
81383-001-01	2023-01-30	C162847	48780-1	f386c64a-46b2-0266-e053-dadaa90a7c1a	b8c9f57e-dd5d-132b-e053-2a95a90a2bef
81383-001-02	2023-01-30	C162847	48780-1	f386c64a-46b2-0266-e053-dadaa90a7c1a	b8c9f57e-dd5d-132b-e053-2a95a90a2bef
81383-001-03	2023-01-30	C162847	48780-1	f386c64a-46b2-0266-e053-dadaa90a7c1a	b8c9f57e-dd5d-132b-e053-2a95a90a2bef
81383-001-04	2023-01-30	C162847	48780-1	f386c64a-46b2-0266-e053-dadaa90a7c1a	b8c9f57e-dd5d-132b-e053-2a95a90a2bef

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
81383-001-01	Dr. Dris Hand Sanitizer	60 mL in 1 BOTTLE	LIQUID	60	1
81383-001-02	Dr. Dris Hand Sanitizer	240 mL in 1 BOTTLE	LIQUID	240	1
81383-001-03	Dr. Dris Hand Sanitizer	475 mL in 1 BOTTLE	LIQUID	475	1
81383-001-04	Dr. Dris Hand Sanitizer	4000 mL in 1 BOTTLE	LIQUID	4000	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
81383-001	DR. DRIS HAND SANITIZER (ETHYL ALCOHOL) LIQUID [HANSON VENTURE ENTERPRISE INC.]	1	Legacy NDC, 4 package rows	20210114_b8c9f57e-dd5d-132b-e053-2a95a90a2bef.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

Dr. Dris Hand Sanitizer
Ethyl Alcohol
WATER
ALOE VERA LEAF
ALCOHOL
HYDROXYETHYL CELLULOSE, UNSPECIFIED
PEPPERMINT OIL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
81383-001	81383-001-01, 81383-001-02, 81383-001-03, 81383-001-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
ALOE VERA LEAF	ZY81Z83H0X	IACT
ALCOHOL	3K9958V90M	ACTIB
HYDROXYETHYL CELLULOSE, UNSPECIFIED	T4V6TWG28D	IACT
PEPPERMINT OIL	AV092KU4JH	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
b8c9f57e-dd5e-132b-e053-2a95a90a2bef			b8c9f57e-dd5d-132b-e053-2a95a90a2bef	2021-01-13	Warnings	Exact identifier spl id: b8c9f57e-dd5e-132b-e053-2a95a90a2bef spl set id: b8c9f57e-dd5d-132b-e053-2a95a90a2bef

Reported adverse events (FAERS/openFDA)#

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