HAND SANITIZER GEL- ethyl alcohol gel 
SPIRIT PHARMACEUTICALS LLC

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.

----------

Dr. SANITIZER HAND SANITIZER gel

Drug Facts

Active ingredient

Ethyl alcohol 70%

Purpose

Antiseptic

Uses

• hand sanitizer to help reduce bacteria on the skin that potentially can cause disease
• recommend for repeated use

Warnings

For external use only. Flammable. Keep away from heat and flame.
Do not use • in 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 appears and lasts. These may be signs of a serious condition.

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

Directions

Other Information

• Store between 15°-30°C (59°86°F)
• Avoid freezing and excessive heat above 40°C (104°F)
• may discolor certain fabrics or surfaces

Inactive ingredients

carbomer, fragrance, glycerin, hydrogen peroxide, propylene glycol, tocopheryl acetate, triethanolamine, water

Questions or comments?

1-888-333-9792

PRINCIPAL DISPLAY PANEL

Dr. SANITIZER

HAND-SANITIZER GEL

EFFECTIVELY KILLS 99.9% OF THE

MOST COMMON GERMS/ BACTERIA

70%

ALCOHOL CONTENT

WITH

VITAMIN E & MOISTURIZERS

PLEASANT FRAGRANCE

STAY PROTECTED

150 ml / 250 ml / 500 ml

image description

image description

image description

HAND SANITIZER GEL 
ethyl alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68210-4081
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
GLYCERIN (UNII: PDC6A3C0OX)  
HYDROGEN PEROXIDE (UNII: BBX060AN9V)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
TROLAMINE (UNII: 9O3K93S3TK)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:68210-4081-1150 mL in 1 BOTTLE; Type 0: Not a Combination Product06/16/2020
2NDC:68210-4081-2250 mL in 1 BOTTLE; Type 0: Not a Combination Product06/16/2020
3NDC:68210-4081-5500 mL in 1 BOTTLE; Type 0: Not a Combination Product06/16/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A06/16/2020
Labeler - SPIRIT PHARMACEUTICALS LLC (179621011)

Revised: 12/2022
Document Id: ef1acc46-6c24-1fd7-e053-2a95a90ae914
Set id: 0beb6d41-e75f-4065-adaa-b5940334fa83
Version: 3
Effective Time: 20221205
 
SPIRIT PHARMACEUTICALS LLC