Home FDA labels eeb44298-3678-344e-e053-2a95a90a8f5f TestoPRO openFDA label record# This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)
Brand name TestoPRO
Generic name AVENA SATIVA, DAMIANA, HAMAMELIS VIRGINIANA, KOREAN GINSENG, POPULUS TREMULOIDES, BARYTA CARBONICA, HEPAR SUIS, NUPHAR LUTEUM, ORCHITINUM SUIS, PHOSPHORICUM ACIDUM, SABAL SERULATA, SELENIUM METALLICUM, TESTOSTERONE, TRIBULUS TERRESTRIS, HORNY GOAT WEED, TONGKAT ALI, FENUGREEK
Manufacturer ProBlen
Product type HUMAN OTC DRUG
SPL set ID de00895d-db6e-4801-9cfe-a6a4d7235986
SPL ID eeb44298-3678-344e-e053-2a95a90a8f5f
Version 2
Effective date 2022-11-30
Source export date 2026-09-28
Source partition 8
Source file https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 05:55:56 Harmonized routes table Harmonized routes ORAL
Harmonized identifier links# Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
Harmonized identifiers page 1 of 1 · 25 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name TestoPRO openfda.brand_name generic name AVENA SATIVA, DAMIANA, HAMAMELIS VIRGINIANA, KOREAN GINSENG, POPULUS TREMULOIDES, BARYTA CARBONICA, HEPAR SUIS, NUPHAR LUTEUM, ORCHITINUM SUIS, PHOSPHORICUM ACIDUM, SABAL SERULATA, SELENIUM METALLICUM, TESTOSTERONE, TRIBULUS TERRESTRIS, HORNY GOAT WEED, TONGKAT ALI, FENUGREEK openfda.generic_name manufacturer name ProBlen openfda.manufacturer_name ndc package 43853-0035-1 openfda.package_ndc ndc product 43853-0035 openfda.product_ndc ndc11 package 43853003501 derived:openfda.package_ndc spl id eeb44298-3678-344e-e053-2a95a90a8f5f id spl set id de00895d-db6e-4801-9cfe-a6a4d7235986 set_id unii J7WWH9M8QS openfda.unii unii CUQ3A77YXI openfda.unii unii 654825W09Z openfda.unii unii 137PC46F89 openfda.unii unii 6P669D8HQ8 openfda.unii unii 4X4HLN92OT openfda.unii unii KM02613O28 openfda.unii unii MUN0TBE4PE openfda.unii unii 3XMK78S47O openfda.unii unii 714LIU3V6D openfda.unii unii MA9CQJ3F7F openfda.unii unii E4GA8884NN openfda.unii unii RQ2CFA7WWJ openfda.unii unii 8GOM182CI3 openfda.unii unii 6EC706HI7F openfda.unii unii T7S323PKJS openfda.unii unii H6241UJ22B openfda.unii
Warnings cross-check# openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Warnings sections page 1 of 1 · 1 matching rows.
warnings Warnings: Not for use on children. If symptoms continue to recur, or if sleeplessness persists continuously for more than two weeks, consult a physician. As with all medicines, if you are pregnant or breast feeding, consult a health professional before using this product. Keep out of the reach of children . In case of overdose, get medical help or contact a Poison Control Center right away. Keep out of the reach of children.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.