FUSONI HAND SANITIZER WITH MOISTURIZER PLUS BLUE- alcohol gel FUSONI HAND SANITIZER WITH MOISTURIZER PLUS- alcohol gel

Fusoni Hand Sanitizer with Moisturizer Plus by

Drug Labeling and Warnings

Fusoni Hand Sanitizer with Moisturizer Plus by is a Otc medication manufactured, distributed, or labeled by Fusoni S.A. de C.V.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Ethyl alcohol 70% v/v

Purpose

Antimicrobial

Uses

Hand sanitizer to decrease bacteria on the skin that could cause disease. Recommended for repeated use.

Warnings

Flammable, keep away from source of heat, fire or flame.
For external use only. Do not inhale or ingest.

When using this product

do not use in or near the eyes; if contact occurs, rinse eyes
thoroughly with water.

avoid contact with broken skin.

Stop use and ask a doctor if

Stop use and ask a doctor if irritation or rash appears and lasts.

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center immediately.

Directions

place enough product in your palm to thoroughly cover your hands and rub them together until dry.
children under 6 years of age should be supervised when using this product.

Other information

do not store above 109°F (43°C).
may discolor certain surfaces or fabrics.

Inactive ingredients

Product 011 "DRUG FACTS Fusoni Hand Sanitizer Plus.jpg":

Water, Hydroxyethylcellulose, PPG-3 Benzyl Ether Myristate, Citric Acid, Phenoxyethanol, Glycerine, Ammonium Hydroxide.

Product 012 "DRUG FACTS Fusoni Hand Sanitizer Plus Blue.jpg":

Water, Hydroxyethylcellulose, PPG-3 Benzyl Ether Myristate, Citric Acid, Phenoxyethanol, Glycerine, Blue 1, Ammonium Hydroxide.

PRINCIPAL DISPLAY PANEL

3.8 L NDC: 79380-011-12

PRINCIPAL DISPLAY PANEL

3.8 L NDC: 79380-012-12

INGREDIENTS AND APPEARANCE

FUSONI HAND SANITIZER WITH MOISTURIZER PLUS BLUE 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79380-012
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.7 L  in 1 L

Inactive Ingredients
Ingredient Name	Strength
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
HYDROXYETHYL CELLULOSE (4000 MPA.S AT 1%) (UNII: ZYD53NBL45)
PPG-3 BENZYL ETHER MYRISTATE (UNII: 8075L58MKO)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
AMMONIA (UNII: 5138Q19F1X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79380-012-11	0.946 L in 1 BOTTLE; Type 0: Not a Combination Product	07/07/2020
2	NDC: 79380-012-12	3.785 L in 1 BOTTLE; Type 0: Not a Combination Product	07/07/2020
3	NDC: 79380-012-13	18.93 L in 1 PAIL; Type 0: Not a Combination Product	07/07/2020
4	NDC: 79380-012-14	208.18 L in 1 DRUM; Type 0: Not a Combination Product	07/07/2020
5	NDC: 79380-012-15	1003.03 L in 1 CONTAINER; Type 0: Not a Combination Product	07/07/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	07/07/2020

FUSONI HAND SANITIZER WITH MOISTURIZER PLUS 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79380-011
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.7 L  in 1 L

Inactive Ingredients
Ingredient Name	Strength
HYDROXYETHYL CELLULOSE (4000 MPA.S AT 1%) (UNII: ZYD53NBL45)
PPG-3 BENZYL ETHER MYRISTATE (UNII: 8075L58MKO)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
AMMONIA (UNII: 5138Q19F1X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79380-011-11	0.946 L in 1 BOTTLE; Type 0: Not a Combination Product	07/07/2020
2	NDC: 79380-011-12	3.785 L in 1 BOTTLE; Type 0: Not a Combination Product	07/07/2020
3	NDC: 79380-011-13	18.93 L in 1 PAIL; Type 0: Not a Combination Product	07/07/2020
4	NDC: 79380-011-14	208.18 L in 1 DRUM; Type 0: Not a Combination Product	07/07/2020
5	NDC: 79380-011-15	1003.03 L in 1 CONTAINER; Type 0: Not a Combination Product	07/07/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	07/07/2020

Labeler - Fusoni S.A. de C.V. (811412535)

Establishment
Name	Address	ID/FEI	Business Operations
Fusoni S.A. de C.V.		811412535	manufacture(79380-011, 79380-012) , pack(79380-011, 79380-012) , label(79380-011, 79380-012)