HANDY ANTIBAC ANTISEPTIC INSTANT GEL HAND SANITIZER- alcohol gel 
Lentus 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.

----------

Handy Antibac Antiseptic Instant Gel Hand Sanitizer

Drug Facts

Active ingredient

Ethyl alcohol 65%

Purpose

Antiseptic

Use

For hand washing to decrease bacteria on the skin

Warnings

For external use only Flammable, keep away from fire or flame.

Do not use

in the eyes.

Stop use and ask a doctor if

  • irritation and redness develop 
  • condition persists for more than 72 hours

Keep out of reach of children.

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

Directions

wet hands thoroughly with product and allow to dry without wiping

Other information

Inactive ingredients

Water, glycerol, aloe vera leaf juice, carbomer, triethanolamine.

Package Labeling:30ml

Label

Package Labeling:60ml

Label2

Package Labeling:500ml

Label3

Package Labeling:1000ml

Label4

HANDY ANTIBAC ANTISEPTIC INSTANT GEL HAND SANITIZER 
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79873-000
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.65 mL  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
TROLAMINE (UNII: 9O3K93S3TK)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:79873-000-0030 mL in 1 BOTTLE; Type 0: Not a Combination Product08/01/2020
2NDC:79873-000-0160 mL in 1 BOTTLE; Type 0: Not a Combination Product08/01/2020
3NDC:79873-000-02500 mL in 1 BOTTLE; Type 0: Not a Combination Product08/01/202010/08/2021
4NDC:79873-000-031000 mL in 1 BOTTLE; Type 0: Not a Combination Product08/01/202010/08/2021
5NDC:79873-000-04500 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product08/01/2020
6NDC:79873-000-051000 mL in 1 POUCH; Type 0: Not a Combination Product08/01/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E08/01/2020
Labeler - Lentus LLC (078554629)

Revised: 10/2021
Document Id: cddc94d4-f068-ac33-e053-2a95a90accce
Set id: 2f7664f8-0e94-4a86-a769-5a9027b5b0b8
Version: 3
Effective Time: 20211008
 
Lentus LLC