Pregnenolone 25 mg Sublingual

FDA Statement of Identity

A Dietary Supplement

Suggested/Recommended/Usage/Directions

Suggeted Usage: As a dietary supplement, adults take 1/2 to 1 tablet daily as directed by your physician ONLY! (May be taken sublingually by allowing tablet to dissolve in mouth or with water or juice.)

Precautions re: Children

KEEP OUT OF REACH OF CHILDREN.

Storage

For optimal storage conditions, store in a cool, dry place. (59(0)-77(0)F/15(0)-25(0)C) (35-65% relative humidity)

General: Product/Version Code

Formula #83088

Precautions re: Pregnant or Nursing or Prescription Medications

DO NOT USE IF PREGNANT OR NURSING.

Formulation re: Does NOT Contain

This product contains NO yeast, wheat gluten, soy protein, milk/dairy, corn, sodium, sugar, starch, artificial coloring, preservatives or flavoring.

Precautions re: All Other

Consult a physician or licensed qualified health care professional before using this product if you have or have a family history of breast cancer, uterine cancer, ovarian cancer, prostate cancer, prostate enlargement, heart disease, low HDL cholesterol ("good cholesterol"), or if you are using any other dietary supplement, prescription drug, or over-the-counter drug. Do not exceed the recommended serving. Exceeding the recommended serving may cause serious adverse health effects. Possible side effects include changes in liver function, acne, hair loss, hair growth on the face (in women), aggressiveness, irritability, and increased levels of estrogen. Discontinue use and call a physician or licensed qualified health care professional immediately if you experience rapid heartbeat, dizziness, blurred vision, or other similar symptoms.

Precautions re: All Other

Tamper resistant package, do not use if outer seal is missing.

Precautions re: All Other

WARNING: NOT FOR USE BY INDIVIDUALS UNDER THE AGE OF 18 YEARS.

General Statements: All Other Content

Meets Douglas Laboratories spec [#83088]. Conforms to USP <2091> for weight. Meets USP <2040> for disintegration.

General Statements: All Other Content

To report any adverse events call 1-800-332-1088.