WM BROWN X ACQUA DI GABRIEL- hand sanitizing mist lmp spray ACQUA DI GABRIAL- hand sanitizing mist lc spray ACQUA DI GABRIAL- hand sanitizing mist herbal spray

Acqua Di Gabrial by

Drug Labeling and Warnings

Acqua Di Gabrial by is a Otc medication manufactured, distributed, or labeled by Nexderma. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Isopropyl Alcohol 75% v/v. Purpose: Antiseptic

Inactive ingredients

Allantoin
Ultra Pure Water
Silver

Use

Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

KEEP OUT OF REACH OF CHILDREN

Adult supervision recommended for children under 6 years old.

Warnings

Keep away form fire and flame.
Flammable
For external use on hands only.
Keep out of eye, ears and mouth.
If contact in eyes, flush thoroughly with water.
Keep out of reach of children.
If swallowed seek medical help immediately or call your poison control center.
Store between 15-30 (58-86F)
Avoid freezing and excessive heat above 40C (104F)
Will damage wood finishes, plastics and some fabrics.

Do not use

• in children less than 2 months of age
• on open skin wounds

Directions

• Dosage: Place enough product on hands to cover all surfaces. Rub hands together until dry.
• Administration:Topoical

Purpose

Purpose: to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Package Label - Principal Display Panel

125 ml NDC: 79930-7106-1

500 ml NDC: 79930-7106-4

125 ml NDC: 79930-7107-1 Lavender Citrus

500 ml NDC: 79930-7107-4 Lavender Citrus

100 ml NDC: 79930-7110-1 WM Brown LMP

INGREDIENTS AND APPEARANCE

WM BROWN X ACQUA DI GABRIEL 
hand sanitizing mist lmp spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79930-7110
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	75 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ALLANTOIN (UNII: 344S277G0Z)	0.03 mL  in 100 mL
SILVER (UNII: 3M4G523W1G)	0.5 mL  in 100 mL
WATER (UNII: 059QF0KO0R)
POMEGRANATE SEED OIL (UNII: 0UI45XV0T6)
LEMON OIL (UNII: I9GRO824LL)
MANDARIN OIL (UNII: NJO720F72R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79930-7110-1	100 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	09/30/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	09/30/2020

ACQUA DI GABRIAL 
hand sanitizing mist lc spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79930-7107
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	75 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ALLANTOIN (UNII: 344S277G0Z)	0.03 mL  in 100 mL
SILVER (UNII: 3M4G523W1G)	0.5 mL  in 100 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79930-7107-1	125 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	09/30/2020
2	NDC: 79930-7107-4	500 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	09/30/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	09/30/2020

ACQUA DI GABRIAL 
hand sanitizing mist herbal spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79930-7106
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	75 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ALLANTOIN (UNII: 344S277G0Z)	0.03 mL  in 100 mL
SILVER (UNII: 3M4G523W1G)	0.5 mL  in 100 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79930-7106-1	125 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	09/30/2020
2	NDC: 79930-7106-4	500 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	09/30/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	09/30/2020

Labeler - Nexderma (079533940)

Establishment
Name	Address	ID/FEI	Business Operations
Nexderma		079533940	manufacture(79930-7106, 79930-7107, 79930-7110) , pack(79930-7106, 79930-7107, 79930-7110) , label(79930-7106, 79930-7107, 79930-7110)