HAND SANITIZER WITH MOISTURIZERS AND VITAMIN E- ethyl alcohol gel
HEB

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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BACK LABEL - DRUG FACTS BOX

ACTIVE INGREDIENT

ETHYL ALCOHOL 62% (ANTISEPTIC)

USES AND DIRECTIONS

USES: TO HELP REDUCE BACTERIA ON THE SKIN.
DIRECTIONS: PUT A SMALL AMOUNT INTO YOUR PALM AND BRISKLY RUB HANDS TOGETHER UNTIL DRY.

WARNINGS

FOR EXTERNAL USE ONLY.IN CASE OF ACCIDENTAL INGESTION, SEEK MEDICAL ASSISTANCE OR CONTACT A POISON CONTROL CENTER IMMEDIATELY.

WHEN USING THIS PRODUCT

AVOID CONTACT WITH EYES. IF CONTACT OCCURS, RINSE WITH WATER. AVOID CONTACT WITH BROKEN SKIN.

STOP USE AND ASK A DOCTOR IF

SKIN IRRITATION OR REDNESS DEVELOPS.

KEEP OUT OF REACH OF CHILDREN

FOR CHILDREN UNDER 6, USE ONLY WITH ADULT SUPERVISION. NOT RECOMMENDED FOR USE ON INFANTS.

OTHER INFORMATION

FLAMMABLE. KEEP AWAY FROM HEAT AND FLAME.

PACKAGE FRONT AND BACK LABELS

8OZ FRONT AND BACK LABELS: HCF8OZ.jpg

HAND SANITIZER WITH MOISTURIZERS AND VITAMIN E
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:37808-225
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	62.0000 mL in 100 mL

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:37808-225-08	237 mL in 1 BOTTLE, PUMP

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333	07/05/2010

Labeler - HEB (007924756)