DNA HAND SANITIZER- alcohol gel 
Welburn Corporation

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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DNA Hand Sanitizer

Drug Facts

Active ingredients

Alcohol 70% v/v

Purpose

Antiseptic

Uses

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

  • 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 thoroughly with water.

Stop use and seek 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, Glycerin, Triethanolamine, Iodopropynyl Butylcarbamate, Methylisothiazolinone.

Questions?

call 888 387 3887

Company Information

Distributed by:

Welburn Corporation

Hermosa Beach, CA 90254

Made in Guatemala

Product Packaging - 500 ML

ADVANCED FORMULA

DNA

HAND

SANITIZER

GEL

70% SUGAR CANE ALCOHOL

NON STERILE SOLUTION

WITH MOISTURIZING INGREDIENTS

16.9 FL. OZ. / 500 ML

dna hand sanitizer

DNA HAND SANITIZER 
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:77622-031
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
GLYCERIN (UNII: PDC6A3C0OX)  
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)  
TROLAMINE (UNII: 9O3K93S3TK)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:77622-031-03236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product11/19/2020
2NDC:77622-031-10500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product11/19/2020
3NDC:77622-031-083785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product11/19/2020
4NDC:77622-031-02119 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product11/19/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A11/19/2020
Labeler - Welburn Corporation (117515830)

Revised: 11/2020
Document Id: b4792d1b-9ecc-11db-e053-2995a90a1d7f
Set id: a57993f6-d7d7-d1cc-e053-2a95a90a3202
Version: 5
Effective Time: 20201119
 
Welburn Corporation