TESTI-DROP

Manufacturer
Groupe Cyrenne Inc.
Effective date
2025-11-20
Label type
OTC ANIMAL DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 02:36:05

Label at a glance#

ProductTESTI-DROP
Active ingredientGOLD, CLEMATIS RECTA FLOWERING TOP, SILICON DIOXIDE, THUJA OCCIDENTALIS LEAFY TWIG, LEAD
Label structure6 sections

Indications and uses

Promotes the descent of the testis inside the scrotum. For cats and dogs only.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Aurum Metallicum 6k, Clematis Erecta 6k, Silicea 6k, Thuja Occidentalis 6k, Plumbum Metallicum 6k

Uses

INDICATIONS & USAGE SECTION

Promotes the descent of the testis inside the scrotum. For cats and dogs only.

Warnings

WARNINGS SECTION

Shake well before use. Respect the dosage. Essential oils can negate the effects of homeopathic products. Store at room temperature. Keep out of reach of children.

Direction

DOSAGE & ADMINISTRATION SECTION

1 spray every day, in water or directly in the mouth. Once the testicle has dropped, keep giving 1 spray a day for one more week to avoid a yo-yo effect. Then stop the product. Not for prevention.

Inactive ingredient

INACTIVE INGREDIENT SECTION

Ethyl alcohol 20%, purified water

Product label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
86147-071-01TESTI-DROP30 mL in 1 BOTTLELIQUID304

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
86147-07186147-071-01

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

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 · 10 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Aurum metallicumGOLDBoiron84629c2b-ce31-bf90-e053-2a91aa0a21f72023-11-08Name fallback
generic name: GOLD
Aurum metallicumGOLDBoiron846272f1-0065-442f-e053-2a91aa0a90a32023-11-08Name fallback
generic name: GOLD
Aurum metallicumGOLDBoiron6b413d60-29d5-11e7-8208-424c583030312023-11-08Name fallback
generic name: GOLD
Aurum metallicumGOLDBoiron84629309-14d4-e597-e053-2991aa0a87e42023-11-08Name fallback
generic name: GOLD
Aurum metallicumGOLDBoiron84f1001f-5cdf-43b2-e053-2a91aa0a273d2023-11-08Name fallback
generic name: GOLD
Aurum metallicumGOLDBoiron84f0ac34-f7e2-16e9-e053-2991aa0a67562023-06-05Name fallback
generic name: GOLD
Aurum metallicumGOLDBoiron84f0f339-5427-b584-e053-2991aa0a220a2023-03-28Name fallback
generic name: GOLD
Aurum metallicumGOLDBoiron84625779-41fd-547e-e053-2991aa0a205a2023-02-20Name fallback
generic name: GOLD
Aurum metallicumGOLDBoiron84f10008-5c27-43b4-e053-2a91aa0a64b92023-02-20Name fallback
generic name: GOLD
Aurum metallicumGOLDBoiron8462be19-1f01-790b-e053-2991aa0ad29d2023-02-20Name fallback
generic name: GOLD

Reported adverse events (FAERS/openFDA)#

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