Fem Response Liquid
FDA Label NDC 64616-091

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Vitality Works, Inc. for the product Fem Response (NDC 64616-091). 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 fem response, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Fem Response

Apocynum Cannabinum 7X                Cuprum Arsenicosum 10X

Aralia Racemosa 15X, 30X                 Lacticum Acidum 10X

Bellis Perennis 10X, 20X                    Sabina 20X

Carica Papata 8C                              Wyethia Heleniodes 30X

Alcohol, Purified Water

Use only under the direction of a health care professional. Do not use if tamper evident seal is broke or missing.

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

For the temporary relief of hot flashes, confusion, irritability, syptoms of premenses, abnormal menstrual function and pelvic pain and discomfort.

Orally 25 drops, 2 times per day or as indicated by a physician. Children 12 and under use one half the adult dosage.

Helps ease hot flashes, confusion, irritability symptoms of premenses, abnormal menstrual function and pelvic pain and discomfort.

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