VANILLA HAND SANITIZER - alcohol liquid 
MGS Group Limited

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.

----------

Vanilla Hand Sanitizer

Active Ingredient

Ethyl Alcohol 62%

Purpose

Sanitizer

Uses

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

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

Hand Sanitizer

VANILLA HAND SANITIZER 
alcohol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:51263-3125
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL62 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
GLYCERIN (UNII: PDC6A3C0OX)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
TOCOPHEROL (UNII: R0ZB2556P8)  
TROLAMINE (UNII: 9O3K93S3TK)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:51263-3125-259 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E06/18/2012
Labeler - MGS Group Limited (663512177)

Revised: 6/2012
Document Id: 4d8dd2ad-f84b-4f4b-92e5-01584491acea
Set id: 235a1292-e008-49ed-8757-a68299abb211
Version: 2
Effective Time: 20120619
 
MGS Group Limited