COCONUT VANILLA HAND SANITIZER- alcohol liquid

Coconut Vanilla Hand Sanitizer by

Drug Labeling and Warnings

Coconut Vanilla Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Unique Holding Group Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient

Ethyl Alcohol 62%  

PURPOSE

Purpose:

Sanitizer

INDICATIONS & USAGE

Uses:

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

WARNINGS

Warnings:

For external use only-hands.
Use only as directed.
Excessive use or prolonged exposure may cause irritation to the skin.
Discontinue use if irritation, redness, or itching occurs.
Flammable. Keep away from heat and flame

WHEN USING

When Using This Product:

Keep out of eyes. In case of contact with eyes, flush immediately with water and call a doctor.

Avoid contact with broken skin

ASK DOCTOR

Stop Use And Ask A Doctor if irritation or redness develops

KEEP OUT OF REACH OF CHILDREN

Keep Out of Reach of Children

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

DOSAGE & ADMINISTRATION

Directions:

Put a thumb size amount in your palm and rub hands together briskly until dry

STORAGE AND HANDLING

Other Information

Do not store in temperatures over 118F

Children under six years of age should be supervised while using this product.

May discolor certain fabrics

INACTIVE INGREDIENT

Inactive Ingredients

aloe barbadensis gel, carbomer, deionized water, Fragrance, glycerin, propylene glycol, D and C Red No. 33, triethanolamine, and vitamin E, FDA and C Yellow No. 5

PRINCIPAL DISPLAY PANEL

labe

INGREDIENTS AND APPEARANCE

COCONUT VANILLA HAND SANITIZER 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 25225-022(NDC:None)
Route of Administration	TOPICAL

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

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)	35.5998 g  in 100 g
Propylene Glycol (UNII: 6DC9Q167V3)	0.5 g  in 100 g
Glycerin (UNII: PDC6A3C0OX)	1 g  in 100 g
ALOE VERA LEAF (UNII: ZY81Z83H0X)	0.01 g  in 100 g
CARBOMER HOMOPOLYMER TYPE C (UNII: 4Q93RCW27E)	0.33 g  in 100 g
ALPHA-TOCOPHEROL (UNII: H4N855PNZ1)	0.01 g  in 100 g
TROLAMINE (UNII: 9O3K93S3TK)	0.35 g  in 100 g
VANILLA (UNII: Q74T35078H)	0.1 g  in 100 g
D&C RED NO. 33 (UNII: 9DBA0SBB0L)	0.0001 g  in 100 g
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)	0.0001 g  in 100 g
COCONUT (UNII: 3RT3536DHY)	0.1 g  in 100 g

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 25225-022-01	28 g in 1 BOTTLE, PLASTIC
2	NDC: 25225-022-02	59 g in 1 BOTTLE, PLASTIC
3	NDC: 25225-022-04	237 g in 1 BOTTLE, PLASTIC
4	NDC: 25225-022-05	500 g in 1 BOTTLE, PLASTIC
5	NDC: 25225-022-03	222 g in 1 BOTTLE, PLASTIC

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	11/13/2010

Labeler - Unique Holding Group Inc (529047265)

Registrant - Unique Holding Group Inc (529047265)

Establishment
Name	Address	ID/FEI	Business Operations
Unique Holding Group Inc		529047265	manufacture