HAND SANITIZER UPSIDE DOWN- alcohol gel 
MERCI HANDY CORPORATION

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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Hand Sanitizer Upside Down

Drug Facts

Active ingredient

Alcohol 67% (v/v)

Purpose

Antiseptic

Use

for handwashing to decrease bacteria on the skin

Warnings

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

Do not use

in the eyes. In case of contact, flush eyes with water.

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

Store at a temperature below 110° F (43° C)

Inactive ingredients

Aqua (Water), Parfum (Fragrance), Aloe Barbadensis Leaf Juice Powder, Glycerin, Propylene Glycol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol, Mannitol, Microcrystalline Cellulose, Sucrose, Zea Mays (Corn) Starch, Denatonium Benzoate, Tocopheryl Acetate, Maltodextrin, Hydroxypropyl Methylcellulose, Potassium Sorbate, Sodium Benzoate, Alpha-Isomethyl Ionone, Citronellol, Geraniol, CI 73360 (Red 30 Lake), CI 42090 (Blue 1), CI 17200 (Red 33).

Package Labeling:72866-035-01

30mL Bottle

Package Labeling:72866-035-02

30mL Bottle with hanger

HAND SANITIZER UPSIDE DOWN 
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72866-035
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL67 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
MALTODEXTRIN (UNII: 7CVR7L4A2D)  
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
ISOMETHYL-.ALPHA.-IONONE (UNII: 9XP4LC555B)  
.BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)  
GERANIOL (UNII: L837108USY)  
D&C RED NO. 30 (UNII: 2S42T2808B)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
WATER (UNII: 059QF0KO0R)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
GLYCERIN (UNII: PDC6A3C0OX)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
MANNITOL (UNII: 3OWL53L36A)  
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
SUCROSE (UNII: C151H8M554)  
CORN (UNII: 0N8672707O)  
DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:72866-035-0130 mL in 1 BOTTLE; Type 0: Not a Combination Product09/20/2021
2NDC:72866-035-021 in 1 CONTAINER09/20/2021
230 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 finalpart333E09/20/2021
Labeler - MERCI HANDY CORPORATION (118006306)

Revised: 12/2022
Document Id: eec8e47f-ebbd-a22f-e053-2995a90a073a
Set id: deaf6024-4b5c-4be8-9a8f-3374fe65175d
Version: 2
Effective Time: 20221201
 
MERCI HANDY CORPORATION