HAND SANITIZER, DOLCE VITA- alcohol gel

Hand Sanitizer, Dolce Vita by

Drug Labeling and Warnings

Hand Sanitizer, Dolce Vita by is a Otc medication manufactured, distributed, or labeled by Merci Handy Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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,Benzyl Salicylate, Linalool, Geraniol, Citronellol, Limonene, FD&C Yellow No. 5, FD&C Red No. 4, Iron Oxides

QUESTIONS OR COMMENTS?

(646)-358-3432

Package Labeling:

INGREDIENTS AND APPEARANCE

HAND SANITIZER, DOLCE VITA 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72866-007
Route of Administration	TOPICAL

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

Inactive Ingredients
Ingredient Name	Strength
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)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
SODIUM BENZOATE (UNII: OJ245FE5EU)
BENZYL SALICYLATE (UNII: WAO5MNK9TU)
LINALOOL, (+/-)- (UNII: D81QY6I88E)
GERANIOL (UNII: L837108USY)
.BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)
LIMONENE, (+)- (UNII: GFD7C86Q1W)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
FD&C RED NO. 4 (UNII: X3W0AM1JLX)
FERRIC OXIDE RED (UNII: 1K09F3G675)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72866-007-30	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/10/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	03/01/2020

Labeler - Merci Handy Corporation (116958007)