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Package insert / prescribing information
Generic name: formaldehyde
Dosage form: topical liquid
Drug class: Miscellaneous topical agents

Medically reviewed by Last updated on May 23, 2022.

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.

Formadon provides a preferable vehicle for the topical application for formalin solution. It is formulated with an aqueous perfumed base which helps minimize the characteristic pungent odor.

2 oz. sponge tip plastic bottle and 4 oz. plastic bottle
Formaldehyde (10% of USP strength) Formulated in aqueous perfumes base.

Use as an antiperspirant in the treatment of severe conditions of hyperhidrosis and bromidosis. Drying agent for verrucae.Apply to feet twice weekly as prescribed by a physician.

For external use only. Keep out of reach of children. Avoid frequent use. Avoid contact with eyes or mucous membranes. Do not apply to open wounds. Should sign of irritation occurs , medication should be discontinued. Irritates eyes, nose and throat. Use with adequate ventilation. In the event of eye contact, flush with copiously with water and get medical attention. Harmful if swallowed. Contact your local poison center immediately. Do not induce vomiting. If conscious, give eight ounces of (240mL) of milk, water with activated charcoal.

Federal law (USA) prohibits dispensing without a prescription.

Keep well closed in a cool place.

formaldehyde liquid
Product Information
Product Type HUMAN PRESCRIPTION DRUG LABEL Item Code (Source) NDC:10481-1050
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Formaldehyde (Formaldehyde) Formaldehyde 0.1 mL in 59 mL
Inactive Ingredients
Ingredient Name Strength
# Item Code Package Description
1 NDC:10481-1050-2 118 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved drug other 06/21/2010
Labeler - Gordon Laboratories (002333847)
Registrant - Gordon Laboratories (002333847)
Name Address ID/FEI Operations
Gordon Laboratories 002333847 manufacture
Gordon Laboratories

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