FDA.reportPublic FDA data

Herbciti Prostazen 180Caps

Manufacturer
HerbCiti LLC
Effective date
2022-01-05
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 22:18:11

Label at a glance#

ProductHerbciti Prostazen 180Caps
Active ingredientSAW PALMETTO, REYNOUTRIA JAPONICA ROOT, RUBIA CORDIFOLIA ROOT
Label structure9 sections

Dosage and administration

Take two (2) capsules three times a day.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Reynoutria japonica Root 20%, Rubia cordifolia Root 15%, Saw Palmetto 3%

Purpose

OTC - PURPOSE SECTION

Reverses enlarged prostate, restores prostatic utricle function, and reverses prostatitis*

Keep Out of Reach of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

Directions

DOSAGE & ADMINISTRATION SECTION

Take two (2) capsules three times a day.

Use

INDICATIONS & USAGE SECTION

  • To reverse enlarged prostate
  • To restore prostatic utricle function
  • To reverse prostatitis

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Goji Berry (Lycium chinense) Fruit, Chinese Asparagus (Asparagus cochinchinensis), Eucommia (Eucommia ulmoides) Bark, Asiatic Plantain (Plantago asiatica), Cinnamon

Warning

WARNINGS SECTION

Individuals with known medical conditions should consult a doctor prior to using this.

Other Information

OTHER SAFETY INFORMATION

Do not use if seal is broken.
Do not eat freshness packet enclosed.
Keep product out of direct sunlight, high temperature, and humidity.

Store in a cool, dry place.

Package Label Display

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Prostazen180Prostazen180HerbCiti Prostazen™

ENLARGED PROSTATE RECOVERY
PROSTATIC UTRICLE FUNCTION RESTORE
PROSTATITIS RECOVERY

Homeopathic 180 Capsules

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
80353-70180353-701-02, 80353-701-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
SAW PALMETTOJ7WWH9M8QSACTIB
ASPARAGUS COCHINCHINENSIS WHOLE36L6R7F7P9IACT
PLANTAGO ASIATICA5F5728J5E8IACT
CINNAMON5S29HWU6QBIACT
LYCIUM CHINENSE FRUITTG711Q7A1QIACT
REYNOUTRIA JAPONICA ROOT7TRV45YZF7ACTIB
RUBIA CORDIFOLIA ROOT4V873H15CGACTIB
EUCOMMIA ULMOIDES BARKL878N1L0ARIACT

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 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
e69f00ea-4881-1faa-e053-2a95a90afa42d4dfcc1b-5861-00b0-e053-2a95a90ac3812022-08-19WarningsExact identifier
spl set id: d4dfcc1b-5861-00b0-e053-2a95a90ac381

Reported adverse events (FAERS/openFDA)#

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