Monsels Solution

Generic Name: ferric subsulfate
Dosage Form: topical liquid

Disclaimer: 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.

Monsels Solution

Light-resistant 2 ml  bottles.

Used as a styptic in its undiluted form.

It should not be used in vesicular, bullous, or exudative (oozing) dermatoses because it may then cause permanent pigmentation on the  skin.  May be harmful  if swallowed. For  external use only.  If  swallowed, do not induce vomiting unless directed to do so by medical personnel. Never give anything by mouth to an unconscious person. Loosen tight clothing such as a collar, tie, belt or waistband. Get medical attention immediately. Keep out of reach of children. 

Restricted to use by or on the order of a licensed Physician. Store at room temperature. Keep cap tightly sealed and protect from light.

Monsels Solution 
ferric subsulfate liquid
Product Information
Product Type HUMAN PRESCRIPTION DRUG LABEL Item Code (Source) NDC:10481-0112
Route of Administration TOPICAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
# Item Code Package Description
1 NDC:10481-0112-2 59 g in 1 BOTTLE, GLASS
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved drug other 12/07/2011
Labeler - Gordon Laboratories (002333847)
Registrant - Gordon Laboratories (002333847)
Name Address ID/FEI Operations
Gordon Laboratories 002333847 manufacture
Revised: 12/2011
Gordon Laboratories

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