HAND SANITIZER, NAMASTE- 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.

----------

Hand Sanitizer, Namaste

Drug Facts

Active ingredient

Alcohol 67%

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

Water (Aqua), Fragrance (Parfum), Aloe Vera Leaf Juice Powder, Glycerin, Propylene Glycol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol, Mannitol, Microcrystalline Cellulose, Sucrose, Corn (Zea Mays) Starch, Denatonium Benzoate, Tocopheryl Acetate, Maltodextrin, Hydroxypropyl Methylcellulose, Potassium Sorbate, Sodium Benzoate, Hexyl Cinnamal, Benzyl Benzoate, Linalool, imonene, Ferric Ferrocyanide, D&C Red No. 33, D&C Red No. 30, FD&C Blue No. 1.

QUESTIONS OR COMMENTS?

(646)-358-3432

Package Labeling:

Bottle3

HAND SANITIZER, NAMASTE
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:72866-002
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	670 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
MANNITOL (UNII: 3OWL53L36A)
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
SUCROSE (UNII: C151H8M554)
STARCH, CORN (UNII: O8232NY3SJ)
DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
SODIUM BENZOATE (UNII: OJ245FE5EU)
.ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I)
BENZYL BENZOATE (UNII: N863NB338G)
LINALOOL, (+/-)- (UNII: D81QY6I88E)
LIMONENE, (+)- (UNII: GFD7C86Q1W)
FERRIC FERROCYANIDE (UNII: TLE294X33A)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)
D&C RED NO. 30 (UNII: 2S42T2808B)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:72866-002-30	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/01/2019

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333E	03/01/2019

Labeler - Merci Handy Corporation (116958007)

Revised: 8/2020

Document Id: acd96d35-da17-1256-e053-2a95a90a9df0

Set id: 0c9bc0c5-42f2-4e63-99e0-2e5c62f7ac6d

Version: 3

Effective Time: 20200814

Merci Handy Corporation