HAND SANITIZER- alcohol gel 
Super Dope Laboratories 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.

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Super Dope Banana

Active Ingredient(s)

Ethyl Alcohol 70% v/v. Purpose: Antiseptic

Purpose

Antiseptic, Hand Sanitizer

Use

Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings

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

Do not use

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

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. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Other information

Inactive ingredients

Water, Carbomer 940, Glycerin, Hydrogen Peroxide, Trolamine, Fragrance

Package Label - Principal Display Panel

3785mL NDC: 74220-004-01

label

HAND SANITIZER 
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:74220-005
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
COUMARIN (UNII: A4VZ22K1WT)  
CINNAMALDEHYDE (UNII: SR60A3XG0F)  
METHYL HEPTINE CARBONATE (UNII: 0TTP6YT2T3)  
HYDROGEN PEROXIDE (UNII: BBX060AN9V)  
CARBOMER 940 (UNII: 4Q93RCW27E)  
GLYCERIN (UNII: PDC6A3C0OX)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:74220-005-013785 mL in 1 BOTTLE; Type 0: Not a Combination Product07/31/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A07/31/2020
Labeler - Super Dope Laboratories LLC (055650002)
Establishment
NameAddressID/FEIBusiness Operations
Super Dope Laboratories LLC055650002manufacture(74220-005) , label(74220-005)

Revised: 8/2020
Document Id: ac39cb90-f186-8faa-e053-2995a90ab67a
Set id: ac39c730-56a8-117b-e053-2a95a90ad4ae
Version: 1
Effective Time: 20200806
 
Super Dope Laboratories LLC