OCEAN HAND SANITIZER- alcohol liquid
Mangiacotti, Inc

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.

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Ocean Hand Sanitizer

ACTIVE INGREDIENT

Ethyl Alcohol 62%

PURPOSE

Antiseptic

USES

To decrease bacteria on the skin that could cause disease.
Recommended for repeated use.

WARNINGS

For external use only - hands.

Flammable.

Keep away from heat and flame.

When using this product.

Keep out of eyes. In case of contact with eyes, flush thoroughly with water.
Do not inhale or ingest.
Avoid contact with broken skin.

Stop use and ask a doctor if

skin irritation develops.

Keep out of reach of children.

In case of accidental ingestion seek professional assistance or contact a Poison Control Center immediately.

DIRECTIONS:

Wet hands thoroughly with product and allow to dry without wiping.
For children under 6, do not use without adult supervision.
Not recommended for infants.

OTHER INFORMATION:

Do not store above 105 degrees F.
May discolor some fabrics.
Harmful to wood finishes and plastics.

INACTIVE INGREDIENTS

Water, Glycerin (naturally occurring palm oil), Acrylates/C10-C30 Alkyl Acrylate Crosspolymer, Aloe Barbadensis Leaf Juice, Polysorbate 20, Propylene Glycol, Aminomethyl Propanol, Fragrance with essential oil, Blue 1, Ext.Violet 2.

Say good-bye to those pesky germs with out plant-derived hand sanitizer. Essential oil and aloe will moisturize your hands while killing 99.9% of many common germs that may cause illness*.

Use anytime, without water or towels.

Mangiacotti

mangiacotti.com

* Effective at eliminating over 99.9% of many common harmful germs and bacteria in as little as 15 seconds.

No animal testing. MADE IN USA

Mangiacotti Florals LLC

Ocean Hand Sanitizer 4 FL OZ / 118ml (42926-121-04)

OCEAN HAND SANITIZER
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:42926-121
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	62 mL in 100 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
CARBOMER COPOLYMER TYPE A (UNII: 71DD5V995L)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
D&C VIOLET NO. 2 (UNII: 350KA7O6HK)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:42926-121-04	118 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/08/2012	01/31/2015

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333E	08/08/2012	01/31/2015

Labeler - Mangiacotti, Inc (078850804)

Registrant - Harrison Specialty Co., Inc. (001000355)

Revised: 1/2017

Document Id: 4532f177-c3db-2060-e054-00144ff8d46c

Set id: 82685c20-b47c-4ec7-a231-d03353dc4b89

Version: 2

Effective Time: 20170103

Mangiacotti, Inc