Guna-fem Solution/ Drops
NDC Package 17089-231-18
Package Information
Guna-fem (adenosinum ciclophosphoricum - lilium tigrinum - melatonin - sus scrofa adrenal gland - sus scrofa corpus luteum - sus scrofa hypothalamus - sus scrofa ovary - sus scrofa pancreas - sus scrofa pineal gland - sus scrofa pituitary gland - sus scrofa thymus - thyroid -) solution/ dropses is take 15 minutes before mealsAdults and children 16 years and older 20 drops in a little water 2 times per dayChildren between 16 years and 8 years of age. 10 drops in a little water 2 times per dayChildren under 8 years Ask a doctor. This formulation utilizes a solution/ drops delivery system. Marketed by Guna Spa, this product is identified by NDC 17089-231.
Identification & Billing
Clinical Specifications
- ADENOSINE CYCLIC PHOSPHATE 6 [hp_X]/30mL
- LILIUM LANCIFOLIUM BULB 6 [hp_X]/30mL
- MELATONIN 200 [hp_X]/30mL
- SUS SCROFA ADRENAL GLAND 30 [hp_X]/30mL
- SUS SCROFA CORPUS LUTEUM 30 [hp_X]/30mL
- SUS SCROFA HYPOTHALAMUS 30 [hp_X]/30mL
- SUS SCROFA OVARY 6 [hp_X]/30mL
- SUS SCROFA PANCREAS 30 [hp_X]/30mL
- SUS SCROFA PINEAL GLAND 30 [hp_X]/30mL
- SUS SCROFA PITUITARY GLAND 30 [hp_X]/30mL
- SUS SCROFA THYMUS 30 [hp_X]/30mL
- THYROID 6 [hp_X]/30mL
Regulatory & Marketing
Hierarchy Structure
- 17089 - Guna Spa
- 17089-231 - Guna-fem
- 17089-231-18 - 1 BOTTLE, DROPPER in 1 BOX / 30 mL in 1 BOTTLE, DROPPER
- 17089-231 - Guna-fem
The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.
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Frequently Asked Questions
What is the distribution configuration for this product package?
The code 17089-231-18 identifies a specific commercial package of 1 bottle, dropper in 1 box / 30 ml in 1 bottle, dropper of Guna-fem, a human over the counter drug labeled by Guna Spa. This solution/ drops is formulated for oral use and contains adenosine cyclic phosphate; lilium lancifolium bulb; melatonin; sus scrofa adrenal gland; sus scrofa corpus luteum; sus scrofa hypothalamus; sus scrofa ovary; sus scrofa pancreas; sus scrofa pineal gland; sus scrofa pituitary gland; sus scrofa thymus; thyroid as the active substance.
Is this product currently listed with the FDA?
Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Guna Spa on May 23, 2006. The current certification is valid through December 31, 2027.
How is this Guna Spa product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 17089023118. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.
11-Digit Code Conversion
Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:
Note: The zero is added to the Product segment to maintain the 5-4-2 structure.