FORMADON- formaldehyde liquid

Formadon by

Drug Labeling and Warnings

Formadon by is a Prescription medication manufactured, distributed, or labeled by Gordon Laboratories. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DESCRIPTION

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

SPL UNCLASSIFIED SECTION

Formaldehyde (10% of USP strength) Formulated in aqueous perfumes base.

INDICATIONS & USAGE

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.

WARNINGS AND PRECAUTIONS

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.

SPL UNCLASSIFIED SECTION

Federal law (USA) prohibits dispensing without a prescription.

SPL UNCLASSIFIED SECTION

Keep well closed in a cool place.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

FORMADON 
formaldehyde liquid

Product Information
Product Type	HUMAN PRESCRIPTION DRUG	Item Code (Source)	NDC: 10481-1050
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Formaldehyde (UNII: 1HG84L3525) (Formaldehyde - UNII:1HG84L3525)	Formaldehyde	0.1 mL  in 59 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 10481-1050-5	59 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)

Establishment
Name	Address	ID/FEI	Business Operations
Gordon Laboratories		002333847	manufacture