DR. DRIS HAND SANITIZER- ethyl alcohol liquid 
Hanson Venture Enterprise Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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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:

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

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

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

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, Aloe Vera Leaf Juice, Hydroxyethyl Cellulose, Peppermint Oil

Questions or Comments?

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

PDP

DR. DRIS HAND SANITIZER 
ethyl alcohol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:81383-001
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL2720 mL  in 4000 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D)  
PEPPERMINT OIL (UNII: AV092KU4JH)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:81383-001-0160 mL in 1 BOTTLE; Type 0: Not a Combination Product01/13/2021
2NDC:81383-001-02240 mL in 1 BOTTLE; Type 0: Not a Combination Product01/13/2021
3NDC:81383-001-03475 mL in 1 BOTTLE; Type 0: Not a Combination Product01/13/2021
4NDC:81383-001-044000 mL in 1 BOTTLE; Type 0: Not a Combination Product01/13/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A01/13/2021
Labeler - Hanson Venture Enterprise Inc. (204263995)
Establishment
NameAddressID/FEIBusiness Operations
Natures Formulae Health Products Ltd.241385587manufacture(81383-001)

Revised: 1/2021
Document Id: b8c9f57e-dd5e-132b-e053-2a95a90a2bef
Set id: b8c9f57e-dd5d-132b-e053-2a95a90a2bef
Version: 1
Effective Time: 20210113
 
Hanson Venture Enterprise Inc.