COLCIGEL

Manufacturer
Gensco Laboratories, LLC
Effective date
2022-10-04
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 02:18:15

Label at a glance#

ProductCOLCIGEL
Active ingredientCOLCHICINE
Label structure12 sections

Indications and uses

ColciGel® transdermal gel is indicated for prophylaxis and the treatment of acute gout flares. Treatment of Gout Flares: ColciGel® gel is indicated for treatment of acute gout flares when used at the first sign of a flare. Prophylaxis of Gout Flares: ColciGel® is indicated for prophylaxis of gout flares.

Dosage and administration

Apply 1 – 4 pumps up to four times per day. 1 application = 1 pump (0.25ml) covers an area 4” in diameter. Children under 16 years of age do not use unless directed by a physician. DISCARD 6 MONTHS AFTER FIRST USE

Storage and handling

ColciGel® is Colchicinum 4X in a transdermal gel base. The gel is viscous and opaque in appearance. ColciGel® is available in 2x15mL sealed dispensing containers that produce 0.25 mL of gel per each manual depression of the plunger top (pump). 2x15mL (1.01 fl oz) Bottles NDC 35781-0400-4 Store at 20° to 25°C (68° to 77°F). [See USP Controlled Room Temperature] DISPENSE IN ORIGINAL CONTAINER. US Patent Pending Manu...

Label contents#

Full prescribing information#

1 INDICATIONS AND USAGE

INDICATIONS & USAGE SECTION

1.1 Gout Flares

SPL UNCLASSIFIED SECTION

ColciGel® transdermal gel is indicated for prophylaxis and the treatment of acute gout flares.

Treatment of Gout Flares:

ColciGel® gel is indicated for treatment of acute gout flares when used at the first sign of a flare.

Prophylaxis of Gout Flares:

ColciGel® is indicated for prophylaxis of gout flares.

2 DOSAGE AND ADMINISTRATION

DOSAGE & ADMINISTRATION SECTION

Apply 1 – 4 pumps up to four times per day.
1 application = 1 pump (0.25ml) covers an area 4” in diameter.

Children under 16 years of age do not use unless directed by a physician.

DISCARD 6 MONTHS AFTER FIRST USE

3 DOSAGE FORMS AND STRENGTHS

DOSAGE FORMS & STRENGTHS SECTION

ColciGel® is Colchicinum 4X in a transdermal gel base. The gel is viscous and opaque in appearance. ColciGel® is available in 15 mL sealed dispensing containers that produce 0.25 mL of gel per each manual depression of the plunger top (pump).

4 CONTRAINDICATIONS

CONTRAINDICATIONS SECTION

Label section

Patients with severe renal or severe hepatic impairment should not be given ColciGel® in conjunction with P-gp or strong CYP3A4 inhibitors (this includes all protease inhibitors, except fosamprenavir). In these patients, life-threatening and fatal colchicine toxicity has been reported with ORAL colchicine taken in therapeutic doses.

5 WARNINGS

WARNINGS SECTION

For External Use Only • Avoid Contact With Eyes and Mouth • Keep Out of Reach of Children Store at 25º C (77º F); exclusions permitted to 15º to 30ºC (59º to 86º F). See USP Controlled Room Temperature


PRECAUTIONS

PRECAUTIONS SECTION

Use in Pregnancy: No human or animal studies on the effect of ColciGel® (colchicinum 4X) in pregnancy have been conducted.


Nursing Mothers: It is not known whether ColciGel® (colchicinum 4X) is excreted in breast milk.

6 ADVERSE REACTIONS

ADVERSE REACTIONS SECTION

Prophylaxis and Treatment of Gout Flares: The most commonly reported adverse reaction in clinical trials for the prophylaxis and treatment of gout was mild skin irritation at the site of application.

7 DRUG INTERACTIONS

DRUG INTERACTIONS SECTION

ColciGel® (Colchicinum 4X) is a substrate of the efflux transporter P-glycoprotein (P-gp). Of the cytochrome P450 enzymes tested, CYP3A4 was mainly involved in the metabolism of colchicinum. If ORAL colchicine is administered with drugs that inhibit P-gp, most of which also inhibit CYP3A4, increased concentrations of colchicinum are likely. Fatal drug interactions have been reported. Topical application of ColciGel® has demonstrated insignificant systemic absorption in animal testing and confirmed in limited human pharmacokinetic evaluations and, therefore, poses a limited risk of clinically significant drug interactions. Physicians should, however, ensure that patients are suitable candidates for treatment with ColciGel® and remain alert for signs and symptoms of toxicities related to increased colchicinum exposure as a result of a drug interaction. Signs and symptoms of ColciGel® toxicity should be evaluated promptly and, if toxicity is suspected, ColciGel® should be discontinued immediately.

12 CLINICAL PHARMACOLOGY

CLINICAL PHARMACOLOGY SECTION

The mechanism by which colchicinum exerts its beneficial effect in patients has not been fully elucidated; however, evidence suggests that colchicinum may interfere with the intracellular assembly of the inflammasome complex present in neutrophils and monocytes that mediates activation of interleukin-1alpha. Additionally, colchicine disrupts cytoskeletal functions through inhibition of alpha-tubulin polymerization into microtubules and consequently prevents the activation, degranulation, and migration of neutrophils thought to mediate some gout symptoms.

13 NONCLINICAL TOXICOLOGY

NONCLINICAL TOXICOLOGY SECTION


CARCINOGENESIS & MUTAGENESIS & IMPAIRMENT OF FERTILITY SECTION

Carcinogenesis

Carcinogenicity studies of colchicinum have not been conducted. Due to the potential for colchicinum to produce aneuploid cells (cells with an unequal number of chromosomes), there is theoretically an increased risk of malignancy..

CARCINOGENESIS & MUTAGENESIS & IMPAIRMENT OF FERTILITY SECTION

Mutagenesis

Colchicine was negative for mutagenicity in the bacterial reverse mutation assay. In a chromosomal aberration assay in cultured human white blood cells, colchicine treatment resulted in the formation of micronuclei. Since published studies demonstrated that colchicine induces aneuploidy from the process of mitotic nondisjunction without structural DNA changes, colchicine is not considered clastogenic, although micronuclei are formed.

CARCINOGENESIS & MUTAGENESIS & IMPAIRMENT OF FERTILITY SECTION

Impairment of Fertility

No studies of colchicinum effects on fertility were conducted with ColciGel®. However, published nonclinical studies demonstrated that colchicine-induced disruption of microtubule formation affects meiosis and mitosis. Reproductive studies also reported abnormal sperm morphology and reduced sperm counts in males, and interference with sperm penetration, second meiotic division, and normal cleavage in females when exposed to colchicine. Colchicine administered to pregnant animals resulted in fetal death and teratogenicity. These effects were dose dependent, with the timing of exposure critical for the effects on embryofetal development. The nonclinical doses evaluated were generally higher than an equivalent human ORAL therapeutic dose, but safety margins for reproductive and developmental toxicity could not be determined. Case reports and epidemiology studies in human male subjects on colchicine therapy indicated that infertility from colchicine is rare. A case report indicated that azoospermia was reversed when therapy was stopped. Case reports and epidemiology studies in female subjects on colchicine therapy have not established a clear relationship between colchicinum use and female infertility. The use of colchicinum needs to be weighed against the potential risks.

14 HOW SUPPLIED/STORAGE AND HANDLING

HOW SUPPLIED SECTION


14.1 How Supplied

SPL UNCLASSIFIED SECTION

ColciGel® is Colchicinum 4X in a transdermal gel base. The gel is viscous and opaque in appearance. ColciGel® is available in 2x15mL sealed dispensing containers that produce 0.25 mL of gel per each manual depression of the plunger top (pump).
2x15mL (1.01 fl oz) Bottles NDC 35781-0400-4

14.2 Storage

STORAGE AND HANDLING SECTION

Store at 20° to 25°C (68° to 77°F).
[See USP Controlled Room Temperature]

DISPENSE IN ORIGINAL CONTAINER.

SPL UNCLASSIFIED SECTION

US Patent Pending

Manufactured for:

Gensco Pharma, LLC

8550 NW 33rd Street, Suite 200.

Miami, FL 33122

(855) 743-6726

www.genscopharma.com

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Box
Box
Label
Label

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
51989a2b-944a-b31f-835e-469c133570adProduct name220250716
11e940b0-77bd-45d4-a80f-028ff6bd67e2Product name220250214
14efe2b0-2695-4943-8b2f-24f519c99fedProduct name120231023
bf4e8ffd-8f13-3050-5248-581676b7ea42Product name620221214
987af351-b977-4822-ac44-c76d29e24e78Product name120190611

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
35781-0400-22023-07-28C16284748780-19d75b9d0-14e6-f424-e053-dadaa90a57ceCOLCIGEL These highlights do not include all the information needed to use colchicine safely and effectively. See full prescribing information for ColciGel ® . Initial U.S. Approval
35781-0400-42023-07-28C16284748780-19d75b9d0-14e6-f424-e053-dadaa90a57ceCOLCIGEL These highlights do not include all the information needed to use colchicine safely and effectively. See full prescribing information for ColciGel ® . Initial U.S. Approval
35781-0400-22022-10-05C16284748780-19d75b9d0-14e6-f424-e053-dadaa90a57ceCOLCIGEL These highlights do not include all the information needed to use colchicine safely and effectively. See full prescribing information for ColciGel ® . Initial U.S. Approval
35781-0400-42022-10-05C16284748780-19d75b9d0-14e6-f424-e053-dadaa90a57ceCOLCIGEL These highlights do not include all the information needed to use colchicine safely and effectively. See full prescribing information for ColciGel ® . Initial U.S. Approval
35781-0400-22022-07-29C16284748780-19d75b9d0-14e6-f424-e053-dadaa90a57ceCOLCIGEL These highlights do not include all the information needed to use colchicine safely and effectively. See full prescribing information for ColciGel ® . Initial U.S. Approval
35781-0400-42022-07-29C16284748780-19d75b9d0-14e6-f424-e053-dadaa90a57ceCOLCIGEL These highlights do not include all the information needed to use colchicine safely and effectively. See full prescribing information for ColciGel ® . Initial U.S. Approval
35781-0400-22020-09-14C16284748780-19d75b9d0-14e6-f424-e053-dadaa90a57ceCOLCIGEL These highlights do not include all the information needed to use colchicine safely and effectively. See full prescribing information for ColciGel ® . Initial U.S. Approval
35781-0400-42020-09-14C16284748780-19d75b9d0-14e6-f424-e053-dadaa90a57ceCOLCIGEL These highlights do not include all the information needed to use colchicine safely and effectively. See full prescribing information for ColciGel ® . Initial U.S. Approval
35781-0400-22020-01-31C16284748780-19d75b9d0-14e6-f424-e053-dadaa90a57ceCOLCIGEL These highlights do not include all the information needed to use colchicine safely and effectively. See full prescribing information for ColciGel ® . Initial U.S. Approval
35781-0400-42020-01-31C16284748780-19d75b9d0-14e6-f424-e053-dadaa90a57ceCOLCIGEL These highlights do not include all the information needed to use colchicine safely and effectively. See full prescribing information for ColciGel ® . Initial U.S. Approval

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
35781-0400-2COLCIGEL15 mL in 1 BOTTLE, DISPENSINGGEL155
35781-0400-2COLCIGEL1 in 1 CARTONGEL15
35781-0400-4COLCIGEL30 mL in 1 BOTTLE, DISPENSINGGEL305
35781-0400-4COLCIGEL2 in 1 PACKAGEGEL25

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
35781-0400COLCIGEL (COLCHICINUM 4X) GEL [GENSCO LABORATORIES, LLC]5Legacy NDC, 4 package rows20221006_dd7806d9-50cf-486b-97ce-afeaef02d699.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
35781-0400-2ML - Milliliter35781-040093333c74-cefe-42ed-8908-95bafb33111f12018-02-20
35781-0400-4ML - Milliliter35781-0400d1e8cd50-326b-401d-8e74-3b46888835ff12015-06-09

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
COLCHICINEACTIVE INGREDIENTSML2Y3J35T1
COLCHICINEACTIVE MOIETYSML2Y3J35T1
DOCUSATE SODIUMINACTIVE INGREDIENTF05Q2T2JA01
ISOPROPYL MYRISTATEINACTIVE INGREDIENT0RE8K4LNJS1
LECITHIN, SOYBEANINACTIVE INGREDIENT1DI56QDM621
UREAINACTIVE INGREDIENT8W8T17847W1
WATERINACTIVE INGREDIENT059QF0KO0R1

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
35781-040035781-0400-4, 35781-0400-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 43 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
ISOPROPYL MYRISTATEISOPROPYL MYRISTATE0RE8K4LNJSAEROSOL / TOPICAL9.3 %w/wExact identifier — unii candidate
18 equally ranked IID candidates
UREAUREA8W8T17847WTABLET, COATED / ORAL0.02 mgExact identifier — unii candidate
7 equally ranked IID candidates
UREAUREA8W8T17847WSYSTEM / TOPICAL840 mgExact identifier — unii candidate
7 equally ranked IID candidates
ISOPROPYL MYRISTATEISOPROPYL MYRISTATE0RE8K4LNJSAEROSOL, SPRAY / TOPICAL6.89 %w/wExact identifier — unii candidate
18 equally ranked IID candidates
ISOPROPYL MYRISTATEISOPROPYL MYRISTATE0RE8K4LNJSSPRAY / TOPICAL3665 mgExact identifier — unii candidate
18 equally ranked IID candidates
UREAUREA8W8T17847WTABLET, EXTENDED RELEASE / ORAL0.01 mgExact identifier — unii candidate
7 equally ranked IID candidates
ISOPROPYL MYRISTATEISOPROPYL MYRISTATE0RE8K4LNJSFILM / TRANSDERMAL58.08 mgExact identifier — unii candidate
18 equally ranked IID candidates
ISOPROPYL MYRISTATEISOPROPYL MYRISTATE0RE8K4LNJSLOTION / TOPICAL50 mgExact identifier — unii candidate
18 equally ranked IID candidates
LECITHIN, SOYBEANSOYBEAN LECITHIN1DI56QDM62TABLET, EXTENDED RELEASE / ORAL20 mgExact identifier — unii candidate
7 equally ranked IID candidates
DOCUSATE SODIUMDOCUSATE SODIUMF05Q2T2JA0TABLET, FILM COATED / ORAL6 mgExact identifier — unii candidate
11 equally ranked IID candidates
UREAUREA8W8T17847WCREAM / VAGINAL0.64 %w/wExact identifier — unii candidate
7 equally ranked IID candidates
ISOPROPYL MYRISTATEISOPROPYL MYRISTATE0RE8K4LNJSSYSTEM / TRANSDERMAL113 mgExact identifier — unii candidate
18 equally ranked IID candidates
DOCUSATE SODIUMDOCUSATE SODIUMF05Q2T2JA0SUSPENSION, EXTENDED RELEASE / ORAL0.77 mgExact identifier — unii candidate
11 equally ranked IID candidates
LECITHIN, SOYBEANSOYBEAN LECITHIN1DI56QDM62TABLET / ORAL8 mgExact identifier — unii candidate
7 equally ranked IID candidates
LECITHIN, SOYBEANSOYBEAN LECITHIN1DI56QDM62POWDER, FOR SUSPENSION / ORAL39 mgExact identifier — unii candidate
7 equally ranked IID candidates
ISOPROPYL MYRISTATEISOPROPYL MYRISTATE0RE8K4LNJSSYSTEM / TOPICAL7 mgExact identifier — unii candidate
18 equally ranked IID candidates
LECITHIN, SOYBEANSOYBEAN LECITHIN1DI56QDM62CAPSULE / ORAL20 mgExact identifier — unii candidate
7 equally ranked IID candidates
UREAUREA8W8T17847WTABLET, EFFERVESCENT / ORAL60 mgExact identifier — unii candidate
7 equally ranked IID candidates
UREAUREA8W8T17847WDOUCHE / VAGINAL8 %w/wExact identifier — unii candidate
7 equally ranked IID candidates
DOCUSATE SODIUMDOCUSATE SODIUMF05Q2T2JA0INJECTION / INTRAMUSCULAR0.02 %w/vExact identifier — unii candidate
11 equally ranked IID candidates
LECITHIN, SOYBEANSOYBEAN LECITHIN1DI56QDM62AEROSOL, METERED / RESPIRATORY (INHALATION)0.1 %w/wExact identifier — unii candidate
7 equally ranked IID candidates
ISOPROPYL MYRISTATEISOPROPYL MYRISTATE0RE8K4LNJSOIL / TOPICAL213 mgExact identifier — unii candidate
18 equally ranked IID candidates
DOCUSATE SODIUMDOCUSATE SODIUMF05Q2T2JA0GRANULE, FOR SUSPENSION, EXTENDED RELEASE / ORAL20 mgExact identifier — unii candidate
11 equally ranked IID candidates
DOCUSATE SODIUMDOCUSATE SODIUMF05Q2T2JA0TABLET, COATED / ORAL1 mgExact identifier — unii candidate
11 equally ranked IID candidates
DOCUSATE SODIUMDOCUSATE SODIUMF05Q2T2JA0SHAMPOO / TOPICAL2 %w/wExact identifier — unii candidate
11 equally ranked IID candidates
DOCUSATE SODIUMDOCUSATE SODIUMF05Q2T2JA0SUSPENSION / ORAL48 mgExact identifier — unii candidate
11 equally ranked IID candidates
ISOPROPYL MYRISTATEISOPROPYL MYRISTATE0RE8K4LNJSCREAM / VAGINAL50 mgExact identifier — unii candidate
18 equally ranked IID candidates
DOCUSATE SODIUMDOCUSATE SODIUMF05Q2T2JA0CAPSULE, EXTENDED RELEASE / ORALNAExact identifier — unii candidate
11 equally ranked IID candidates
ISOPROPYL MYRISTATEISOPROPYL MYRISTATE0RE8K4LNJSGEL / TOPICAL29 mgExact identifier — unii candidate
18 equally ranked IID candidates
LECITHIN, SOYBEANSOYBEAN LECITHIN1DI56QDM62TABLET, FILM COATED / ORAL0.33 mgExact identifier — unii candidate
7 equally ranked IID candidates
DOCUSATE SODIUMDOCUSATE SODIUMF05Q2T2JA0TABLET / ORAL50 mgExact identifier — unii candidate
11 equally ranked IID candidates
ISOPROPYL MYRISTATEISOPROPYL MYRISTATE0RE8K4LNJSAEROSOL, FOAM / TOPICAL144 mgExact identifier — unii candidate
18 equally ranked IID candidates
ISOPROPYL MYRISTATEISOPROPYL MYRISTATE0RE8K4LNJSFILM, EXTENDED RELEASE / TRANSDERMAL20.4 mgExact identifier — unii candidate
18 equally ranked IID candidates
DOCUSATE SODIUMDOCUSATE SODIUMF05Q2T2JA0CAPSULE / ORAL8.2 mgExact identifier — unii candidate
11 equally ranked IID candidates
ISOPROPYL MYRISTATEISOPROPYL MYRISTATE0RE8K4LNJSCREAM / TOPICAL65000 mgExact identifier — unii candidate
18 equally ranked IID candidates
ISOPROPYL MYRISTATEISOPROPYL MYRISTATE0RE8K4LNJSGEL, METERED / TRANSDERMAL50 mgExact identifier — unii candidate
18 equally ranked IID candidates
ISOPROPYL MYRISTATEISOPROPYL MYRISTATE0RE8K4LNJSOIL / AURICULAR (OTIC)36 mgExact identifier — unii candidate
18 equally ranked IID candidates
LECITHIN, SOYBEANSOYBEAN LECITHIN1DI56QDM62CREAM / VAGINAL1 %w/wExact identifier — unii candidate
7 equally ranked IID candidates
ISOPROPYL MYRISTATEISOPROPYL MYRISTATE0RE8K4LNJSGEL / TRANSDERMAL85 mgExact identifier — unii candidate
18 equally ranked IID candidates
ISOPROPYL MYRISTATEISOPROPYL MYRISTATE0RE8K4LNJSOINTMENT / TOPICAL35 %w/wExact identifier — unii candidate
18 equally ranked IID candidates
DOCUSATE SODIUMDOCUSATE SODIUMF05Q2T2JA0GEL / TOPICAL6 mgExact identifier — unii candidate
11 equally ranked IID candidates
UREAUREA8W8T17847WINSERT / VAGINAL50 mgExact identifier — unii candidate
7 equally ranked IID candidates
ISOPROPYL MYRISTATEISOPROPYL MYRISTATE0RE8K4LNJSSUSPENSION / AURICULAR (OTIC)0.02 %w/wExact identifier — unii candidate
18 equally ranked IID candidates

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
ea3b3d7c-ca55-260b-e053-2995a90a7624dd7806d9-50cf-486b-97ce-afeaef02d6992022-10-04Warnings, Adverse reactionsExact identifier
spl id: ea3b3d7c-ca55-260b-e053-2995a90a7624
spl set id: dd7806d9-50cf-486b-97ce-afeaef02d699

Reported adverse events (FAERS/openFDA)#

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