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Female Stimulant

Generic: Aconiticum Acidum, Cis-, Apis Venenum Purum, Aquilegia Vulgaris, Bovista, Cypripedium Pubescens, Estradiol, Faecalis (Alkaligenes), Folliculinum, Funiculus Umbilicalis Suis, Glandula Suprarenalis Suis, Heart (Suis), Hydrastis Canadensis, Hypophysis Suis, Kreosotum, Lachesis Mutus, Lilium Tigrinum, Magnesia Phosphorica, Mercurius Solubilis, Mutabile Bacillus (Bach), Oophorinum (Suis), Petroselinum Sativum, Pineal Gland (Suis), Placenta Totalis Suis, Progesterone, Sepia, Testosterone, Uterus (Suis)

OTC
Estradiol Congeners✓ FDA-verified
View full FDA label ↗
Female Stimulant is used for temporary relief of symptoms like low sex drive, fatigue, and general female support. It works based on homeopathic principles, which means it aims to help the body restore balance. You take it by placing 1 to 10 drops under your tongue three times a day, or as your health professional advises, with a maximum of 30 drops daily. If you are pregnant or breastfeeding, it's important to consult a health professional before using it. Additionally, keep it out of reach of children and contact a physician or Poison Control Center right away in case of an overdose.
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Uses

  • female support. fatigue. low sex drive.
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Dosage

Take 1-10 drops under the tongue, 3 times a day.
Consult a physician for use in children under 12 years of age.
Always follow your doctor's specific instructions for your dose.
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Side effects

Common

Possible mild symptoms include fatigue and low sex driveIn case of overdosecontact a physician or Poison Control Center
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Warnings

⚠ Important warnings

  • If pregnant or breastfeeding, ask a health professional before use.
  • Keep out of reach of children.
  • Do not use if seal is broken or missing.

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Answers pulled from the FDA label only.

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Medical Disclaimer: This content is provided for informational and educational purposes only and is not intended as medical advice. Always consult a qualified healthcare provider before taking any medication.
Data Source: Publicly available drug labeling information from the U.S. Food and Drug Administration (FDA).