DIPPIN DOTS ALCOHOL FREE HAND SANITIZER- benzalkonium chloride gel 
Flex Beauty Labs

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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DIPPIN DOTS ALCOHOL FREE HAND SANITIZER

Active Ingredients

Benzalkonium Chloride 0.13%.........Antibacterial

Purpose

Antibacterial

Use

To decrease bacteria on the skin and clean hands.

Recommended for repeated uses.

Safety Instructions

For extemal use only.

Do not Eat Or Drink

Flammable.Keep away from fire and flame.

When using this product

In case of contact,rinse eyes thoroughly with water.

Do not use

Do  not use in or near eyes.

KEEP OUT OF REACH OF CHILDREN

If accidentally swallowed, seek medical help or contact Poison Control  center right away.

Inactive Ingredients

Water (aqua), Polysorbate-20, PEG-40 Hydrogenated,Triethanolamine, Carbomer, Fragrance, Glycerin. Propylene Glycol, Calcium Sodium Borosilicate , Titanium Dioxide , Aloe Barbdensis Leaf Juice,Tocopheryl Acetate, Methylchloroisothiazolinone,Methylsothiazolinone ,Blue 1

Yellow 5,Red 9.

Directions

dippin2

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DIPPIN DOTS ALCOHOL FREE HAND SANITIZER 
benzalkonium chloride gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72308-026
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.13 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
POLYSORBATE 20 (UNII: 7T1F30V5YH)  
POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)  
TROLAMINE (UNII: 9O3K93S3TK)  
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
GLYCERIN (UNII: PDC6A3C0OX)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:72308-026-792 in 1 PACKAGE08/03/2020
179 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E08/03/2020
Labeler - Flex Beauty Labs (080858917)

Revised: 8/2020
Document Id: ac0d4e25-3bd3-7131-e053-2a95a90aecac
Set id: bc3be834-77d8-4861-b673-bc760a1e36e4
Version: 2
Effective Time: 20200804
 
Flex Beauty Labs