VANILLA HAND SANITIZER WITH VITAMIN E AND ALOE- ethyl alcohol liquid

Vanilla Hand Sanitizer with Vitamin E and Aloe by

Drug Labeling and Warnings

Vanilla Hand Sanitizer with Vitamin E and Aloe by is a Otc medication manufactured, distributed, or labeled by Papermates, Inc. dba Noteworthy. 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

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

SPL UNCLASSIFIED SECTION

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

PRINCIPAL DISPLAY PANEL

Vanilla Hand Sanitizer

with Moisturizers

Vitamin E and Aloe

Net 2 fl oz (59ml)

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

VANILLA HAND SANITIZER WITH VITAMIN E AND ALOE 
ethyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75997-026
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 (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 Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75997-026-02	59 mL in 1 BOTTLE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	02/02/2011

Labeler - Papermates, Inc. dba Noteworthy (038734620)