HAND SANITIZER- alcohol spray

Hand Sanitizer by

Drug Labeling and Warnings

Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by HAAN BRAND SL, Laboratorios Magrina SL. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Uses

Uses

* To decrease bacterias on the hand. Recommended for repeated use.

Active Ingredient

Active Ingredient Purpose

• Ethyl Alcohol 65%...................................Antiseptic

Warnings

• For external use only- hands
• When using this product keep out o f eyes. In case of contact, flush throughly with water.
• Do Not Inhale or ingest.
• Avoid contact with broken skin
• Keep out of reach of children. In case of incidental ingestion seek professional assistance or contact a Poison Control Center inmediately.
• Stop use and ask Doctor: if skin irritation develops.
• Flammable: Keep away from heat and flame.

Stop use and ask a doctor if

Stop use and ask a doctor if

* Irritation develops

Keep out of reach of children

Keep out of reach of children. In case of incidental ingestion, see professional advice or contact a Poison Control Center inmediately.

Directions

Directions: Wet hands throughly with product and allow to dry without wiping

• For Children under 6 years of age do not use without supervision of an adult. Not recomended for infants

Inactive Ingredients

Water, Water, C10-30 Alkyl Acrylate Crosspolymer, Parfum(Fragrance), Limonene, Tromethamine, Linalool, Hexyl Cinnamal, Potassium Sorbate, Citral, Sodium Benzoate

Questions?

QUESTIONS OR COMMENTS: Visit Haanready.com

Uses

Uses

* To decrease bacterias on the hand. Recommended for repeated use.

Hand Sanitizer Gel

INGREDIENTS AND APPEARANCE

HAND SANITIZER 
alcohol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79091-010
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
CARBOMER 934 (UNII: Z135WT9208)
METHYL GLUCETH-10 (UNII: N0MWT4C7WH)
WATER (UNII: 059QF0KO0R)
LIMONENE, (+)- (UNII: GFD7C86Q1W)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
LINALOOL, (+)- (UNII: F4VNO44C09)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
CITRAL (UNII: T7EU0O9VPP)
SODIUM BENZOATE (UNII: OJ245FE5EU)
.ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I)
TROMETHAMINE (UNII: 023C2WHX2V)
BUTYL ACRYLATE/C16-C20 ALKYL METHACRYLATE/METHACRYLIC ACID/METHYL METHACRYLATE COPOLYMER (UNII: 7K68DGG29P)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79091-010-01	30 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	07/18/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	07/18/2020

Labeler - HAAN BRAND SL (468886727)

Registrant - HAAN BRAND SL (468886727)

Establishment
Name	Address	ID/FEI	Business Operations
Laboratorios Magrina SL		460356033	manufacture(79091-010)

Establishment
Name	Address	ID/FEI	Business Operations
HAAN BRAND SL		468886727	label(79091-010)