HAND SANITIZING WIPES- alcohol cloth

Hand Sanitizing Wipes by

Drug Labeling and Warnings

Hand Sanitizing Wipes 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                                 Purpose

Ethyl Alcohol 62%                               Sanitizer

DESCRIPTION

Uses:

To decrease bacteria on the skin that could cause diseases

Recommended for repeated use

WARNINGS

Warnings:

For external use only-hands. Use only as directed.  Excessive use or prolonged exposure may cause irritation to skin. Discontinue use if rash, redness, or itching occurs.

Flammable. Keep away from heat and flame.

WHEN USING

    When using this product

• Keep out of eyes. In case of contacting with eyes, immediately flash with water and call a doctor.
• Avoid contacting with a broken skin.
  

STOP USE

Stop using 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.

INDICATIONS & USAGE

Directions

Adults and children two years and over:

• Apply to hands
• Allow skin to dry without wiping
  

STORAGE AND HANDLING

        Other Information

• Do not store in temperatures over 118F
  
• Children under six years of age should be supervise while using this product.
  
• May discolor certain fabrics.

INACTIVE INGREDIENT

Inactive Ingredients

water, glycerin, carbomer, triethanolamine, aloe barbadensis extract, and vitamin E

PRINCIPAL DISPLAY PANEL

labe

PRINCIPAL DISPLAY PANEL

outer

INGREDIENTS AND APPEARANCE

HAND SANITIZING WIPES 
alcohol cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 25225-016(NDC:None)
Route of Administration	TOPICAL

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

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)	36.955
Glycerin (UNII: PDC6A3C0OX)	1
ALOE VERA LEAF (UNII: ZY81Z83H0X)	0.005
CARBOMER HOMOPOLYMER TYPE C (UNII: 4Q93RCW27E)	0.02
ALPHA-TOCOPHEROL (UNII: H4N855PNZ1)	0.005
TROLAMINE (UNII: 9O3K93S3TK)	0.015

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 25225-016-01	1 in 1 POUCH
2	NDC: 25225-016-02	2 in 1 POUCH
3	NDC: 25225-016-03	10 in 1 POUCH
4	NDC: 25225-016-04	20 in 1 POUCH

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333	05/03/2010

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