Your browser does not support JavaScript! LUGOLS SOLUTION (LUGOLS) LIQUID [GORDON LABORATORIES]
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RxNorm Names

LUGOLS SOLUTION (lugols) liquid
[Gordon Laboratories]


Category DEA Schedule Marketing Status
HUMAN PRESCRIPTION DRUG LABEL unapproved drug other
NOTE:THIS DRUG HAS NOT BEEN FOUND BY FDA TO BE SAFE AND EFFECTIVE, AND THIS LABELING HAS NOT BEEN APPROVED BY FDA. For further information about unapproved drugs, click here.
Drug Label Sections

Strong Iodine Solution USP a topical anti-infective agent.


Applied with a q-tip.

May be stored at room temperature.

Single use only. Do not reuse.  Discard after one  use. Do not use if  seal is broken. Restricted to use by or on the order of a licensed Physician. Keep cap tightly sealed and product from light.



Image of Lugols Labels

LUGOLS SOLUTION 
lugols liquid
Product Information
Product TypeHUMAN PRESCRIPTION DRUG LABELItem Code (Source)NDC:10481-0111
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
IODINE (IODINE) IODINE0.4 g  in 1 g
Inactive Ingredients
Ingredient NameStrength
POTASSIUM IODIDE 
WATER 
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:10481-0111-88 g in 1 BOTTLE, GLASS
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other02/01/2010
Labeler - Gordon Laboratories (002333847)
Registrant - Gordon Laboratories (002333847)
Establishment
NameAddressID/FEIBusiness Operations
Gordon Laboratories002333847manufacture

Revised: 2/2010
 
Gordon Laboratories

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