Active Ingredients
Progesterone 6X
Progesterone Liquid
FDA Label NDC 43857-0120
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Bioactive Nutritional, Inc. for the product Progesterone (NDC 43857-0120). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredients, indications, warnings, directions, inactive ingredients, keep out of reach of children, indications and usage, questions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Indications
For temporary relief of aching legs, backache, mood swings, painful menses, painful breasts, headaches, hot flashes, and nervousness.
Warnings
If pregnant or breast-feeding, ask a health professional before use.
Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.
Do not use if tamper evident seal is broken or missing.
Store in cool, dry place.
Directions
10 drops orally, 3 times a day. Consult a physician for use in children under 12 years of age.
Inactive Ingredients
Demineralized water, 25% Ethanol.
Keep Out Of Reach Of Children
KEEP OUT OF REACH OF CHILDREN. In case of overdose, get medical help or contact a Poison Control Center right away.
Indications And Usage
For temporary relief of aching legs, backache, mood swings, painful menses, painful breasts, headaches, hot flashes, and nervousness.
Questions
Distributed by:
BIOACTIVE NUTRITIONAL
Melbourne, FL 32935
For Nutritional Information write:
BioActive Nutritional, Inc.
1803 N. Wickham Rd.
Melbourne, FL 32935
Package Label Display
BIOActive Nutritional
PROGESTERONE 6X
HOMEOPATHIC
1 FL OZ (30 ml)* Please review the disclaimer below.
