Your browser does not support JavaScript! FRESH UP ANTISEPTIC HAND (ALCOHOL) SPRAY [G&G MEDICAL PRODUCTS LLC]
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FRESH UP ANTISEPTIC HAND (alcohol) spray
[G&G Medical Products LLC]


Category DEA Schedule Marketing Status
HUMAN OTC DRUG LABEL OTC monograph not final
NOTE: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.
Drug Label Sections

Active ingredient

Ethyl Alcohol 70 percent

Purpose

Antiseptic

Uses

For hand washing to decrease bacteria on the skin.

Warnings

Flammable, keep away from fire or flame

For external use only.

Do not use

  • in the eyes
  • In case of eye contact, flush eyes with water.
Stop use and ask a doctor if irritation and redness develop.

Keep out of reach of children.

If swallowed, get medical help or contact Poison Control Center right away.


Directions

Spray enough product to thoroughly cover and wet hands. Rub hands together until dry. Children under 6 years of age should be supervised when using product.

Other information

Do not store above 40 degree Celsius (100 degree Fahrenheit).

Inactive ingredients

fragrance, glycerin, tocopheryl acetate, water

Package labeling

Kills Germs

NDC 53859-001-00

Fresh Up TM

Antiseptic Hand Sanitizer Spray

Over 150 Sprays!

0.6 FL OZ (18 ml)

Antiseptic Hand Sanitizer Spray

Peel away for Drug Facts

DISTRIBUTED BY:
G AND G MEDICAL PRODUCTS, LLC
P.O BOX 37, DEERFIELD STREET, NJ 08313
UNITED STATES

MADE IN CHINA
www.gandgmed.com


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Outside of back label


FRESH UP ANTISEPTIC HAND 
alcohol spray
Product Information
Product TypeHUMAN OTC DRUG LABELItem Code (Source)NDC:53859-001
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (ALCOHOL) ALCOHOL70 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
GLYCERIN 
.ALPHA.-TOCOPHEROL ACETATE 
WATER 
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:53859-001-0018 mL in 1 CARTRIDGE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E11/07/2012
Labeler - G&G Medical Products LLC (078645725)

Revised: 11/2012
 
G&G Medical Products LLC

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