VANILLA HAND SANITIZER WITH VITAMIN E AND ALOE - ethyl alcohol liquid 
Papermates, Inc. dba Noteworthy

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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Vanilla Hand Sanitizer with Vitamin E and Aloe

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, blue 1, carbomer, deionized water, fragrance, glycerin, propylene glycol, red 33, triethanolamine, vitamin E

Warning this item is for external use only. Do not ingest.


Use anytime, anyplace, without water

Feel refreshed without stickiness or residue


Manufactured for Noteworthy

2010 Noteworthy
Chatsworth, CA 91311

Made in China

Vanilla Hand Sanitizer

with Moisturizers

Vitamin E and Aloe

Net 2 fl oz (59ml)

Vanilla with Aloe Hand Sanitizer

VANILLA HAND SANITIZER WITH VITAMIN E AND ALOE 
ethyl alcohol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:75997-026
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 (UNII: V5VD430YW9)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
TROLAMINE (UNII: 9O3K93S3TK)  
ALPHA-TOCOPHEROL (UNII: H4N855PNZ1)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:75997-026-0259 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A02/02/2011
Labeler - Papermates, Inc. dba Noteworthy (038734620)

Revised: 2/2011
Document Id: 57ca0e0a-2d23-4ada-bf4a-e82e080a67d7
Set id: c9f84957-c22c-48b5-98be-7682a2d15e16
Version: 1
Effective Time: 20110202
 
Papermates, Inc. dba Noteworthy