HANDS FIRST TM- benzalkonium chloride spray 
Hands First, 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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Drug Facts

Active Ingredient

Benzalkonium Chloride 0.13%

Purpose

Antimicrobial

Use

Warnings

Stop use and ask a doctor if:

Direction

Other information

Inactive ingredients

water, cocamidopropyl betaine , allantoin, glycolic acid, dimethicone, aloe vera leaf, lavender extract, colloidal silver, tetrasodium EDTA, phenoxyethanol, ethylhexyl glycerine.

Questions?

Call 1-800-603-0589 between 9am and 5pm (EST) Monday through Friday or visit www.handsfirst.com

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Hands First

4 in 1 action

Alcohol Free Spray

Hand Sanitizer

Doctor created and hospital tested

Sanitize anytime, anywhere

Temporarily protect minor cuts and scrapes

Hydrate your skin

Clean without water

Kills 99.99% of germs

4 fl oz (118mL)

foam
HANDS FIRST TM 
benzalkonium chloride spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:81858-042
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.3 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
ALLANTOIN (UNII: 344S277G0Z)  
GLYCOLIC ACID (UNII: 0WT12SX38S)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
SILVER (UNII: 3M4G523W1G)  
ENGLISH LAVENDER OIL (UNII: ZBP1YXW0H8)  
EDETATE SODIUM (UNII: MP1J8420LU)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:81858-042-16473 mL in 1 BOTTLE; Type 0: Not a Combination Product05/07/2021
2NDC:81858-042-0259 mL in 1 BOTTLE; Type 0: Not a Combination Product05/07/2021
3NDC:81858-042-04118 mL in 1 BOTTLE; Type 0: Not a Combination Product05/07/2021
4NDC:81858-042-07207 mL in 1 BOTTLE; Type 0: Not a Combination Product05/07/2021
5NDC:81858-042-08236 mL in 1 BOTTLE; Type 0: Not a Combination Product05/07/2021
6NDC:81858-042-12354 mL in 1 BOTTLE; Type 0: Not a Combination Product05/07/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E05/07/2021
Labeler - Hands First, LLC. (117961848)
Registrant - Hands First, LLC. (117961848)
Establishment
NameAddressID/FEIBusiness Operations
Hands First, LLC.117961848MANUFACTURE(81858-042)

Revised: 10/2021
Document Id: b073b1a6-59f8-4a6d-944f-84451d093180
Set id: 8d2ef71b-b020-498e-b2eb-5fc52018ba5b
Version: 2
Effective Time: 20211028
 
Hands First, LLC.