SOLGREAT ALCOHOL-FREE FOAMING HAND SANITIZER- benzalkonium chloride spray 
PANATURAL USA, INC.

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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SolGreat Alcohol-Free  Hand Sanitizer 

Active lngredient  

Benzalkonium Chloride

Purpose 

Antibacterial

Uses

Warnings  

For external use only.

When using this product, do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water,

Stop use and ask a doctor if redness or irritation develop and persist for more than 72 hours.

Directions

Inactive Ingredients

cetrimonium chloride citric acid, cocamidopropyl betaine, cocamidopropylamine oxide, glycerin, propylene glycol, tocopheryl acetate, water.

Keep out of reach of children.


Children must be supervised in use of this product.

Other information

To prevent discoloration, avoid contact with clothing.

Product Label - 60 mL SolGreat Alcohol-Free Hand Sanitizer Spray

60mL

Product  Label- 354mL SolGreat Alcohol-Free Foaming Hand Sanitizer

354ml

SOLGREAT ALCOHOL-FREE FOAMING HAND SANITIZER 
benzalkonium chloride spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73913-002
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
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
COCAMIDOPROPYLAMINE OXIDE (UNII: M4SL82J7HK)  
GLYCERIN (UNII: PDC6A3C0OX)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:73913-002-0160 mL in 1 BOTTLE; Type 0: Not a Combination Product03/28/2020
2NDC:73913-002-02354 mL in 1 BOTTLE; Type 0: Not a Combination Product03/28/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A03/28/2020
Labeler - PANATURAL USA, INC. (029572239)
Establishment
NameAddressID/FEIBusiness Operations
Hefei Yatai Daily-Use Chemical Industry Co., Ltd654641724manufacture(73913-002)

Revised: 3/2020
Document Id: 3d005f5e-06da-429d-84ca-18140440abc7
Set id: baf6ffa6-721e-444c-bbcf-5b6164ab219b
Version: 1
Effective Time: 20200327
 
PANATURAL USA, INC.