FDA.reportPublic FDA data

GUNA FEMALE SUPPORT

Manufacturer
Guna spa
Effective date
2021-02-12
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:14:23

Label at a glance#

ProductGUNA FEMALE SUPPORT
Active ingredientLILIUM LANCIFOLIUM WHOLE FLOWERING, SUS SCROFA OVARY, SEPIA OFFICINALIS JUICE, ADENOSINE CYCLIC PHOSPHATE, SUS SCROFA PITUITARY GLAND, SUS SCROFA HYPOTHALAMUS, SUS SCROFA ADRENAL GLAND, SUS SCROFA PANCREAS, MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE, PULSATILLA VULGARIS
Label structure10 sections

Indications and uses

Temporarily relieves symptoms of female hormonal imbalance, such as: mood swings menstrual irregularities menstrual cramps.

Dosage and administration

Take 15 minutes before meals. Adults and children 12 years and older: 20 drops in a little water, 2 times per day Children under 12 years: consult a physician

Label contents#

Full prescribing information#

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

Take 15 minutes before meals.

Adults and children 12 years and older: 20 drops in a little water, 2 times per day

Children under 12 years: consult a physician

ACTIVE INGREDIENTS/PURPOSE

OTC - ACTIVE INGREDIENT SECTION

Adenosinum cylclophosphoricum 6X Relieves mood swings

Glandula suprarenalis suis 30X Relieves menstrual pain

Hypophysis suis 30X Supports ovary function, fertility

Hypothalamus suis 30X Supports endocrine function

Lilium tigrinum 6X Relieves menstrual pain

Magnesia phosphorica 10X Relieves menstrual pain

Oophorinum 6X Supports ovary function, fertility

Pancreas suis 30X Supports menstrual regularity

Pulsatilla 8X Supports menstrual regularity

Sepia officinalis 10X Supports menstrual regularity

USES

OTC - PURPOSE SECTION

Temporarily relieves symptoms of female hormonal imbalance, such as:

  • mood swings
  • menstrual irregularities
  • menstrual cramps.

INACTIVE INGREDIENT SECTION

Inactive ingredient: Ethyl alcohol 30%.

QUESTIONS

OTC - QUESTIONS SECTION

Questions?

info@gunainc.com

Tel. (484) 223-3500


WARNINGS

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

INDICATIONS & USAGE SECTION

Take 15 minutes before meals.

PREGNANCY

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding ask a health care profesisonal before use.

WARNINGS

WARNINGS SECTION

  • Stop use and ask doctor if symptoms worsen or persist more than 5 days.
  • If pregnant or breast-feeding ask a health care professional before use.
  • Keep out of reach of children.
  • In case of accidental overdose, seek professional assistance or contact a poison control center immediately
  • Contains ethyl alcohol 30%

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

5usfeb5usfeb

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6e3c022f-0786-43f1-8857-edff89d5153fProduct name120260309
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c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
17089-501-18GUNA FEMALE SUPPORT1 in 1 BOXSOLUTION/ DROPS11
17089-501-18GUNA FEMALE SUPPORT30 mL in 1 BOTTLE, DROPPERSOLUTION/ DROPS301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
17089-501GUNA FEMALE SUPPORT (LILIUM LANCIFOLIUM WHOLE FLOWERING - SUS SCROFA OVARY - SUS SCROFA PITUITARY GLAND - SEPIA OFFICINALIS JUICE - ADENOSINE CYCLIC PHOSPHATE - PULSATILLA VULGARIS - SUS SCROFA HYPOTHALAMUS - SUS SCROFA ADRENAL GLAND - SUS SCROFA PANCREAS - MAGNESIUM PHOSPHATE DIBASIC TRIHYDRATE) SOLUTION/ DROPS [GUNA SPA]1Current NDC, Legacy NDC, 2 package rows20210217_bb22182f-a503-433f-e053-2995a90a2f47.zip

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
17089-50117089-501-18

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
LILIUM LANCIFOLIUM WHOLE FLOWERINGX67Z2963PIACTIB
SUS SCROFA OVARYS7YTV04R8OACTIB
ALCOHOL3K9958V90MIACT
SEPIA OFFICINALIS JUICEQDL83WN8C2ACTIB
ADENOSINE CYCLIC PHOSPHATEE0399OZS9NACTIB
SUS SCROFA PITUITARY GLANDL0PFEMQ1DTACTIB
SUS SCROFA HYPOTHALAMUSN6R0856Z79ACTIB
SUS SCROFA ADRENAL GLAND398IYQ16YVACTIB
SUS SCROFA PANCREAS9Y3J3362RYACTIB
MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATEHF539G9L3QACTIB
PULSATILLA VULGARISI76KB35JEVACTIB

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
GUNA FEMALE SUPPORTLILIUM LANCIFOLIUM WHOLE FLOWERING - SUS SCROFA OVARY - SUS SCROFA PITUITARY GLAND - SEPIA OFFICINALIS JUICE - ADENOSINE CYCLIC PHOSPHATE - PULSATILLA VULGARIS - SUS SCROFA HYPOTHALAMUS - SUS SCROFA ADRENAL GLAND - SUS SCROFA PANCREAS - MAGNESIUM PHOSPHATE DIBASIC TRIHYDRATEGuna spabb22182f-a503-433f-e053-2995a90a2f472021-02-12WarningsExact identifier
ndc (package): 17089-501-18
ndc (product): 17089-501
ndc11 (package): 17089050118
spl id: bb2217fc-c752-20b1-e053-2995a90a2562
spl set id: bb22182f-a503-433f-e053-2995a90a2f47

Reported adverse events (FAERS/openFDA)#

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