DIPPIN DOTS ALCOHOL FREE HAND SANITIZER- benzalkonium chloride gel

DIPPIN DOTS ALCOHOL FREE HAND SANITIZER by

Drug Labeling and Warnings

DIPPIN DOTS ALCOHOL FREE HAND SANITIZER by is a Otc medication manufactured, distributed, or labeled by Flex Beauty Labs. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

• apply palmful to hands.
• rub hands together vigorously until dry.
• supervise children in the use of this product.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DIPPIN DOTS ALCOHOL FREE HAND SANITIZER 
benzalkonium chloride gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72308-026
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.13 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
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 Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72308-026-79	2 in 1 PACKAGE	08/03/2020
1		79 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	08/03/2020

Labeler - Flex Beauty Labs (080858917)