DR. DRIS HAND SANITIZER- ethyl alcohol liquid

Dr. Dris Hand Sanitizer by

Drug Labeling and Warnings

Dr. Dris Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Hanson Venture Enterprise Inc, Natures Formulae Health Products Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredient

Ethyl Alcohol 68% v/v

Purpose

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

Uses

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

Warnings

For external use only.
Flammable. Keep away from heat or flame.

DO NOT USE

Do not use:

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

WHEN USING

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

STOP USE

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

KEEP OUT OF REACH OF CHILDREN

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

Directions

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

store in a cool dry place. Do not overheat.

Inactive Ingredients

Purified Water, Hydroxyethyl Cellulose, Coconut Pulp Extract, Lavender Oil, Eucalyptus Oil, Aloe Vera Leaf Juice,

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DR. DRIS HAND SANITIZER 
ethyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 81383-002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	2720 mL  in 4000 mL

Inactive Ingredients
Ingredient Name	Strength
HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D)
LAVENDER OIL (UNII: ZBP1YXW0H8)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
WATER (UNII: 059QF0KO0R)
COCONUT (UNII: 3RT3536DHY)
EUCALYPTUS OIL (UNII: 2R04ONI662)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 81383-002-01	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/26/2021
2	NDC: 81383-002-02	240 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/26/2021
3	NDC: 81383-002-03	475 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/26/2021
4	NDC: 81383-002-04	4000 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/26/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	03/26/2021

Labeler - Hanson Venture Enterprise Inc (204263995)

Establishment
Name	Address	ID/FEI	Business Operations
Natures Formulae Health Products Ltd.		241385587	manufacture(81383-002)