Progesterone Combo
Progesterone Combo is an FDA drug label for the active ingredient PROGESTERONE manufactured by Nutritional Specialties, Inc. administered by ORAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20230427.
- Generic name
- PROGESTERONE
- Manufacturer
- Nutritional Specialties, Inc.
- Product type
- HUMAN OTC DRUG
- Route
- ORAL
- Dosage form
- N/A
- NDC
- 83027-0073
- Application
- N/A
- Label effective
- 20230427
Active ingredients
Indications & Usage
INDICATIONS Homeopathic support for hormonal balance.† †Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
Dosage & Administration
DIRECTIONS: Adults: 2 to 3 sprays orally, three times daily. Children under twelve one half adult dosage. Do not take within 15 minutes of consuming food, beverage or brushing teeth. Consult a physician for use in children under 12 years of age.
Contraindications
Not available.
Warnings
WARNINGS: Professional Use Only If pregnant or breast-feeding, ask a health professional before use. In case of overdose, get medical help or contact a Poison Control Center right away. If condition worsens, seek medical attention. KEEP OUT OF REACH OF CHILDREN Do not use if tamper evident seal is broken or missing. Store in a cool place after opening
Adverse Reactions
Not available.