HAND SANITIZER WITH MOISTURIZERS AND VITAMIN E- alcohol liquid

Hand Sanitizer by

Drug Labeling and Warnings

Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Family Dollar Services Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient

Ethyl Alcohol 65%

PURPOSE

Purpose
Antiseptic

INDICATIONS & USAGE

Uses hand sanitizer to help reduce bacteria on the skin. recommended for repeated use

WARNINGS

Warnings Flammable Keep away from fire or flame For external use only

WHEN USING

When using this product avoid contact with eyes in case of eye contact immediately flush eyes with water, call a doctor avoid contact with broken skin

Discontinue use if irritation or redness develops. If condition persists for more than 72 hours, consult a doctor.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. Children should only use this product under adult supervision.

Do not drink. Not edible. In case of accidental ingestion, seek professional assistance or contact a Poison Control Center right away.

SPL UNCLASSIFIED SECTION

Other Information do not store above 105F. May discolor some fabrics Harmful to wood finishes and plastics

DOSAGE & ADMINISTRATION

Directions place enough product in your palm to thoroughly spread on both hands and rub into the skin until dry recommended for repeated use.

INACTIVE INGREDIENT

Inactive ingredients aloe barbadensis leaf extract, caprylyl glycol, carbomer, dimethicone, fragrance, phenoxyethanol, propylene glycol, tocopheryl acetate, triethanolamine, water.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

HAND SANITIZER  WITH MOISTURIZERS AND VITAMIN E
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 55319-505
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	65 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
DIMETHICONE (UNII: 92RU3N3Y1O)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
TROLAMINE (UNII: 9O3K93S3TK)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 55319-505-34	10 mL in 1 BOTTLE, SPRAY

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	10/01/2012

Labeler - Family Dollar Services Inc. (024472631)