Credentials & compliance
Every credential and regulatory document below is published in full and unaltered. Read each document for the authorized animals, use, conditions, and limitations.
- FDA Emergency Use Authorized
- FDA Index (Minor Species)
- GMP compliance
- ISO 9001
FDA Emergency Use Authorized products
Two F10® products are authorized by the U.S. FDA under Emergency Use Authorization for the prevention and treatment of infestations caused by New World Screwworm (Cochliomyia hominivorax) larvae — myiasis. Per the FDA Fact Sheets, the authorized animals are:
- Cattle
- Horses
- Minor species of hoof stock
- Raptors & other wild birds
- Pet birds
- Captive & captured wild, exotic & zoo mammals
F10® Antiseptic Wound Spray with Insecticide
FDA EUA No. 006672
Original EUA authorized March 10, 2026
F10® Antiseptic Barrier Ointment with Insecticide
FDA EUA No. 006677
Original EUA authorized April 24, 2026
Important: It is a violation of Federal law to use these products other than as directed in the FDA Fact Sheet. An Emergency Use Authorization is authorized only for the duration of the emergency declaration, unless revoked sooner. Read each Fact Sheet for the authorized animals, use, conditions, and limitations.
FDA Index of Legally Marketed New Animal Drugs for Minor Species
Four F10® treatment products are listed on the FDA Index for Minor Species. Per each FOI Summary, they are indexed for use in: Raptors, pet birds, captive small mammals, captive reptiles, and captive exotic/zoo mammals. Use is prohibited in dogs, cats, horses, and food-producing species.
Note: the FDA Index listing and the FDA Emergency Use Authorization are two different FDA pathways with different authorized animals. The Index listings above cover minor/exotic species only; the EUA additionally covers cattle, horses, and hoof stock for the screwworm emergency. Each document states its own authorized animals.
Quality & manufacturing standards
F10® products are manufactured by Health and Hygiene (Pty) Ltd under recognised quality-management and good-manufacturing-practice systems. Certificates are published in full.
Credentials — questions & answers
- Are F10® products FDA-approved?
- Two F10® products carry an FDA Emergency Use Authorization (EUA) for New World Screwworm, and four F10® treatment products are listed on the FDA Index of Legally Marketed New Animal Drugs for Minor Species. An EUA and an Index listing are specific FDA regulatory pathways; they are not the same as full FDA new-animal-drug approval. Every document is published in full below.
- What is the FDA Index for Minor Species?
- The FDA Index of Legally Marketed New Animal Drugs for Minor Species lets certain drugs be legally marketed for minor (non-major, non-food-producing) species. F10® listings cover raptors, pet birds, captive small mammals, captive reptiles, and captive exotic/zoo mammals, and are prohibited in dogs, cats, horses, and food-producing species. Each listing’s conditions are set out in its FOI Summary.
- What is an FDA Emergency Use Authorization (EUA)?
- An EUA is an FDA authorization for the emergency use of a product during a declared emergency. The F10® EUAs cover the prevention and treatment of New World Screwworm (Cochliomyia hominivorax) myiasis and are authorized only for the duration of the emergency declaration, unless revoked sooner. The authorized animals and conditions are stated in each Fact Sheet.
Verified F10®. Ready to source it?
F10® is supplied through authorized US distributors — one for the FDA Emergency Use Authorized products, one for the rest of the range.
Find a distributor