Equine Sports Council

Controlled Medications Library

ESC MEDICATION CLASSIFICATIONClass A - Therapeutic

ESC Medication Library · Revision 3

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Diclofenac,
Voltaren, Surpass

Medication Facts

Performance enhancing
No
Total hours to clear
40
Frequently used
Most Prescribed
ESC ID
DICLOF-0289
Trade names
Voltaren
Drug type
NSAID
Plasma half-life · hours
5 to 8
Equine dosing
0.2–0.4 mg/kg 5 " ribbon
Cmax · peak plasma concentration
1 ng/mL
Tmax · time to peak plasma concentration
2 hours
ESC concentration guidance
0.8 mcg/mL to 1.0 ng/mL
Primary withdrawal · hours
6
Washout withdrawal · hours
0
ESC control type
A1 - Generally Controlled - Therapeutic
Medication report required
Generally not required, however understand exceptions.

Uses & side effects

Pain, inflamation relief for bones/joints topical cream no GI issues

The label lists possible NSAID reactions including weight loss, colic, diarrhea and jaundice; stop use and contact the veterinarian if these occur. Topical administration can still result in systemic exposure. Avoid concurrent NSAIDs or corticosteroids. See the full product label in Government Numbers.

Drug interactions

When used as a topical cream (the common equine form), it provides localized relief for roughly 6 to 12 hours. Systemic (oral/injectable) use is less common in horses due to gastric toxicity risks. Using more than one NSAID concurrently (e.g., combining phenylbutazone, flunixin meglumine, or firocoxib) drastically increases risks of toxicity without increasing pain relief.Corticosteroids (e.g., Dexamethasone): Combining NSAIDs with steroids increases the likelihood of gastric ulcers and severe GI toxicity.Nephrotoxic Agents: Avoid combining NSAIDs with aminoglycoside antibiotics (e.g., gentamicin) or diuretics, as this significantly increases the risk of acute renal failure.Blood Thinners: Concomitant use with anticoagulants (e.g., heparin) increases the risk of bleeding complications.Dehydration/Pre-existing Disease: NSAIDs are more toxic when horses are dehydrated, septic, or have pre-existing kidney or hepatic disease

Contraindications

Diclofenac, DMSO

Government Numbers

Surpass diclofenac sodium 1% topical cream: NADA 141-186; NDC 0010-4498-01 (124 g tube). Labeler: Boehringer Ingelheim Animal Health USA Inc. Identifiers apply to Surpass cream. DailyMed label updated April 6, 2026; reviewed September 18, 2026. Full label: https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=567de37c-c9da-46e7-8347-01a832ee21b2

Sanctioning-body comparison

Plasma only. Compare published competition guidance for this medication. ESC guidance remains in Medication Facts above. A dosing guideline, withdrawal recommendation and laboratory detection threshold are different measures.

Sources reviewed September 23, 2026. “Not verified” means a gap in this comparison, not zero tolerance or permission. Doses describe the cited rules; your veterinarian must determine treatment and withdrawal.

Published guidance by organization
OrganizationPublished dose & routePlasma concentrationWithdrawal / timingControl / penalty class
AQHA Show HorsesShow rules · 2026 handbook
Conditions & sources

One permitted NSAID at a time. Flunixin emergency exception requires veterinary examination, reporting and 24 h out of competition. Guidelines do not guarantee a compliant result.

VIO404–406; VIO405.2

Reviewed 2026-09-23

73 mg liposomal cream to one site every 12 h; maximum 146 mg/day, up to 10 days.0.005 µg/mL12 hQuantitatively restricted therapeutic NSAID.
APHA Paint Show HorsesShow rules · 2026 Rule Book
Conditions & sources

APHA’s published dosing guidance is not a numerical plasma allowance. Government restrictions and all SC-085 conditions still apply.

SC-085.A.6

Reviewed 2026-09-23

73 mg liposomal cream to one site every 12 h; maximum 146 mg/day, up to 10 days.No numeric plasma limit stated in SC-085.A.No drug-specific precompetition stop time stated in SC-085.A.Listed permitted therapeutic substance.
ARCI Model RulesRacing model · Rules 15 / UCG 20.0 / CTMS 4.2.1
Conditions & sources

ARCI model comparison only; no state-specific rule is substituted. Schedule timing is tied to its stated regimen and is not a clearance guarantee.

CTMS 4.2.1 revision record; UCG 20.0 PDF p. 24

Reviewed 2026-09-23

Removed from CTMS; no allowed dosing regimen inferred.Laboratory detection limit; no numeric allowed plasma value in CTMS 4.2.1.No permitted-use withdrawal guideline in this schedule.Drug Class 4 · Penalty Class C. Removed from CTMS; detection-based restriction.
USEFNational Therapeutic Substance Provisions · 2026 + July amendment
Conditions & sources

Therapeutic Substance Provisions only. One permitted NSAID at a time; additional permitted NSAIDs need the source’s 3-day interval. Emergency exceptions and other restrictions apply. Guidelines do not guarantee clearance.

GR410.4; NSAID guidelines

Reviewed 2026-09-23

73 mg liposomal cream to one site every 12 h; maximum 146 mg/day, up to 10 days.0.005 µg/mL12 hRestricted therapeutic NSAID under GR410.