FDA.reportPublic FDA data

Gy-Na-Tren

Manufacturer
Natren Inc.
Effective date
2021-11-18
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 22:26:47

Label at a glance#

ProductGy-Na-Tren
Active ingredientLACTOBACILLUS ACIDOPHILUS, ASCORBIC ACID, BORIC ACID, WOOD CREOSOTE, SODIUM BORATE, PULSATILLA PRATENSIS, CALENDULA OFFICINALIS FLOWERING TOP, ECHINACEA ANGUSTIFOLIA, THUJA OCCIDENTALIS LEAFY TWIG
Label structure10 sections

Storage and handling

keep dry and refrigerated tamper evident: do not use if seal on bottle is broken

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

​Boricum acidum 3X 120 mg HPUS (Boric Acid)

​Calendula officinalis​ 1X 120 mg HPUS (Marigold)

​Echinacea angustifolia​ 1X 120 mg HPUS (Coneflower)

​Thuja occidentalis​ 1X 120 mg HPUS (Arborvitae)

​Borax veneta​ 3X 27 mg HPUS (Borate of Sodium)

​Kreosotum​ 12X 27 mg HPUS (Beechwood Kreosote)

​Pulsatilla pratensis​ 30X 27 mg HPUS (Wind Flower)

OTC - PURPOSE SECTION

Boricum acidum 3X 120 mg HPUS (Boric Acid)

Calendula officinalis 1X 120 mg HPUS (Marigold)

Echinacea angustifolia 1X 120 mg HPUS (Coneflower)

Thuja occidentalis 1X 120 mg HPUS (Arborvitae)

Borax veneta 3X 27 mg HPUS (Borate of Sodium)

Kreosotum 12X 27 mg HPUS (Beechwood Kreosote)

Pulsatilla pratensis 30X 27 mg HPUS (Wind Flower)

For the relief of external and internal irritation, burning, itching, and discharge associated with vaginal yeast overgrowth.^

The letters "HPUS" indicate that the component in this product is officially monographed in the Homeopathic Pharmacopoeia of the United States.

INDICATIONS & USAGE SECTION

Temporarily relieves symptoms associated with vaginal yeast overgrowth.^

WARNINGS SECTION

For vaginal use only.

OTC - DO NOT USE SECTION

Do not

  • ingest
  • use while using a tampon
  • use if you are pregnant or suspect you are pregnant
  • use if you have a known hypersensitivity to any ingredient in the product

OTC - ASK DOCTOR SECTION

Ask a doctor before use if you

  • experiencing pelvic or vaginal pain
  • are having a high fever
  • are experiencing vaginal discharge with a foul smell
  • are under a doctor's care for any serious condition
  • have a sexually tansmitted disease (STD), pelvic inflammatory disease (PID), or urinary tract infection (UTI)

OTC - STOP USE SECTION

Stop use and ask a doctor if you experience

  • vaginal pain
  • high fever
  • severe irritation or burning
  • vaginal discharge with a foul smell
  • symptoms persisting for more than 14 days or if they clear up and occur again within a few days
  • a worsening condition

OTC - PREGNANCY OR BREAST FEEDING SECTION

​If pregnant or breast feeding, ask a health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

​Keep out of reach of children.

DOSAGE & ADMINISTRATION SECTION

(for complete directions see insert)

  • Wash hands before use
  • when vaginal area is clean and dry, using your index finger, gently insert V-capsul into your vagine as far as comfortable
  • adults and children over 12 years of age: insert one capsule daily before bedtime
  • repeat for 14 consecutive days
  • the use of a panty liner is recommended during the application of this product
  • children under 12 years of age: consult a doctor

STORAGE AND HANDLING SECTION

  • keep dry and refrigerated
  • tamper evident: do not use if seal on bottle is broken

INACTIVE INGREDIENT SECTION

Cellulose powder, coconut oil powder, dehydrated potato powder, gelatin, hypromellose, sodium ascorbate, sodium phosphate.

OTC - QUESTIONS SECTION

call 1.800.992.3323 between 7am and 4pm Pacific Time

DESCRIPTION SECTION

^Indications based on Homeopathic Materia Medica for self limiting conditions.

These statements have not been evaluated by the Food and Drug Administration.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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Products#

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

DailyMed product names page 1 of 1 · 23 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
32267-94032267-940-14
32267-94132267-941-14

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 21 matching rows.

Name, UNII, Kind table
NameUNIIKind
POWDERED CELLULOSESMD1X3XO9MIACT
LEUCINEGMW67QNF9CIACT
POTATOCFE1S8DYWDIACT
CHICKPEAN91637DNW9IACT
HYPROMELLOSE, UNSPECIFIED3NXW29V3WOIACT
LACTOBACILLUS ACIDOPHILUS1PRR1V42V5ACTIB
ASCORBIC ACIDPQ6CK8PD0RACTIB
POWDERED CELLULOSESMD1X3XO9MIACT
GELATIN2G86QN327LIACT
HYPROMELLOSE, UNSPECIFIED3NXW29V3WOIACT
COCONUT OILQ9L0O73W7LIACT
POTATOCFE1S8DYWDIACT
SODIUM ASCORBATES033EH8359IACT
SODIUM PHOSPHATESE337SVY37IACT
BORIC ACIDR57ZHV85D4ACTIB
WOOD CREOSOTE3JYG22FD73ACTIB
SODIUM BORATE91MBZ8H3QOACTIB
PULSATILLA PRATENSIS8E272251DIACTIB
CALENDULA OFFICINALIS FLOWERING TOP18E7415PXQACTIB
ECHINACEA ANGUSTIFOLIAVB06AV5US8ACTIB
THUJA OCCIDENTALIS LEAFY TWIG1NT28V9397ACTIB

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
26bea504-4b46-4f27-e063-6394a90a21ddcee7ff01-dd91-4f9b-86e0-4ac4d7a99c2a2024-11-12WarningsExact identifier
spl set id: cee7ff01-dd91-4f9b-86e0-4ac4d7a99c2a

Reported adverse events (FAERS/openFDA)#

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