VANILLA HAND SANITIZER- alcohol liquid

Vanilla Hand Sanitizer by

Drug Labeling and Warnings

Vanilla Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by MGS Group Limited. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Ethyl Alcohol 62%

Purpose

Sanitizer

Uses

• to decrease bacteria on the skin that could cause disease
• recommended for repeated use
  

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 this product

• keep out of eyes. In case of contact with eyes, immediately flush with water and call a doctor.
• avoid contact with broken skin.
  

Stop use and ask a doctor if

irritation or redness develops

Keep out of reach of children.

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

Directions

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

Other Information

• do not store in temperatures over 118F
• Children under 6 years of age should be supervised while using this product
• may discolor certain fabrics
  

Inactive Ingredients

aloe barbadensis gel, carbomer, fragrance, glycerin, propylene glycol, tocopherol, triethanolamine, water.

Product Labeling

Vanilla Hand Sanitizer

net 2 fl oz (59mL)

Drug Facts Inside

Hand Sanitizer - Vanilla

Manufactured for MGS
MGS Group, Ltd.

2012 MGS Group, Ltd
2229 Barry Avenue
Los Angeles, CA 90064
Made in China

INGREDIENTS AND APPEARANCE

VANILLA HAND SANITIZER 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 51263-3125
Route of Administration	TOPICAL

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

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
TOCOPHEROL (UNII: R0ZB2556P8)
TROLAMINE (UNII: 9O3K93S3TK)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 51263-3125-2	59 mL in 1 BOTTLE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	06/18/2012

Labeler - MGS Group Limited (663512177)