Monsels Solution

Generic Name: ferric subsulfate

Dosage Form: topical liquid
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 NDC Product Code (Source) 10481-0112 Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength FERRIC SUBSULFATE (FERRIC SUBSULFATE) FERRIC SUBSULFATE .21 g  in 1 g

Inactive Ingredients Ingredient Name Strength No Inactive Ingredients Found

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 10481-0112-2 59 g In 1 BOTTLE, GLASS None

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)

Establishment
Name	Address	ID/FEI	Operations
Gordon Laboratories		002333847	manufacture

Revised: 12/2011Gordon Laboratories

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