Forma-Ray

Manufacturer
Gordon Laboratories
Effective date
2010-07-15
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:52:17

Label at a glance#

ProductForma-Ray
Active ingredientFormaldehyde
Label structure8 sections

Label contents#

Full prescribing information#

DESCRIPTION SECTION

A tinted aqueous perfumed base provides preferable vehicles for the topical application of  formalin solution

to relieve severe conditions of bromidrosis and hyperhydrosis. This formula is double the strength of Formadon.

Formalin solution dries the skin's surface , and makes a very good drying agent after surgery or laser treatment.

HOW SUPPLIED SECTION

FORMA-RAY.jpg

2 oz sponge tip plastic bottle and 4oz plastic bottle

SPL UNCLASSIFIED SECTION


Formaldehyde (20% of USP strength) formulated in in aqueous perfumed base.

INDICATIONS & USAGE SECTION

Indications: Antiperspirant for the treatment of hyperhydrosis and bromidrosis. Drying agent for verrucae.

Drying agent for post surgical removal of warts or for nonsurgical laser treatment of warts.

Directions: Apply to feet twice weekly or as prescribed by a Physician.

WARNINGS AND PRECAUTIONS SECTION

Contraindications/Warnings:  Avoid frequent use. Avoid contact with eyes or mucous membranes.

Do not apply to open wounds. should signs of irritation develop, medications should be discontinued. Irritates eyes,nose and throat.

Keep out of reach of children.For external use only. Harmful if swallowed. Contact your local poison control center immediately.

Do not induce vomiting.  If conscious, give eight ounces of (240mL) of milk, water or water with activated charcoal.

SPL UNCLASSIFIED SECTION

Federal law prohibits dispensing without prescription.

SPL UNCLASSIFIED SECTION

Keep well closed in a cool place.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of Forma-Ray label
Image of Forma-Ray label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
10481-3015-52021-11-10C16284748780-1960f7f55-ca55-8e05-e053-dbdaa90a074aFORMA-RAY
10481-3015-52019-10-29C16284748780-1960f7f55-ca55-8e05-e053-dbdaa90a074aFORMA-RAY

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
10481-3015-2ML - Milliliter10481-30152c533450-e63c-499d-9290-6d7c8684333f12012-07-24
10481-3015-5ML - Milliliter10481-3015315f79ce-e7f6-4dca-82d0-2b7e02e24eb012012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
FormaldehydeACTIVE INGREDIENT1HG84L35251
FormaldehydeACTIVE MOIETY1HG84L35251
WATERINACTIVE INGREDIENT059QF0KO0R1

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
10481-301510481-3015-5

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
NameUNIIKind
Formaldehyde1HG84L3525ACTIB
WATER059QF0KO0RIACT

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
d04caa29-acfc-55f8-e053-2a95a90aede574a85045-d668-4c98-8302-099a063cca3a2021-11-08WarningsExact identifier
spl set id: 74a85045-d668-4c98-8302-099a063cca3a

Reported adverse events (FAERS/openFDA)#

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