Formadon

Manufacturer: Gordon Laboratories
Effective date: 2010-06-21
Label type: HUMAN PRESCRIPTION DRUG LABEL
Version: 9
Source: legacy-cache
Hydrated at: 2026-08-02 01:52:17

Label at a glance#

ProductFormadon

Active ingredientFormaldehyde

Label structure7 sections

Label contents#

Full prescribing information#

DESCRIPTION SECTION

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.

HOW SUPPLIED SECTION

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 SECTION

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 SECTION

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.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
10481-1050-5	2021-11-06	C162847	48780-1	960f7f55-d7de-8e05-e053-dbdaa90a074a	FORMADON
10481-1050-5	2019-10-29	C162847	48780-1	960f7f55-d7de-8e05-e053-dbdaa90a074a	FORMADON

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
10481-1050-2	ML - Milliliter	10481-1050	c40b05d2-2196-42e0-ae1f-9ab0ca59bf8d	1	2012-07-24
10481-1050-5	ML - Milliliter	10481-1050	a0b67c62-fcbc-4b22-aca3-ece0012befdb	1	2012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
Formaldehyde	ACTIVE INGREDIENT	1HG84L3525	9
Formaldehyde	ACTIVE MOIETY	1HG84L3525	9
WATER	INACTIVE INGREDIENT	059QF0KO0R	9

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 3 matching rows.

Formadon
Formaldehyde
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
10481-1050	10481-1050-5

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
Formaldehyde	1HG84L3525	ACTIB
WATER	059QF0KO0R	IACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
d00efd93-aa07-42ee-e053-2995a90a802c			36b221c6-4318-4e2a-8cd0-d5558b04cdc6	2021-11-05	Warnings	Exact identifier spl set id: 36b221c6-4318-4e2a-8cd0-d5558b04cdc6

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.