NDC 17089-231

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 -

GUNA-FEM is a Oral Solution/ Drops in the Human Otc Drug category. It is labeled and distributed by Guna Spa. The primary component is Adenosine Cyclic Phosphate; Sus Scrofa Corpus Luteum; Sus Scrofa Adrenal Gland; Sus Scrofa Pituitary Gland; Sus Scrofa Hypothalamus; Lilium Lancifolium Bulb; Melatonin; Sus Scrofa Ovary; Sus Scrofa Pancreas; Sus Scrofa Pineal Gland; Sus Scrofa Thymus; Thyroid.

Product ID17089-231_7dc6a745-863e-c924-e053-2a91aa0aa183
NDC17089-231
Product TypeHuman Otc Drug
Proprietary NameGUNA-FEM
Generic NameAdenosinum 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 -
Dosage FormSolution/ Drops
Route of AdministrationORAL
Marketing Start Date2006-05-23
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameGuna spa
Substance NameADENOSINE CYCLIC PHOSPHATE; SUS SCROFA CORPUS LUTEUM; SUS SCROFA ADRENAL GLAND; SUS SCROFA PITUITARY GLAND; SUS SCROFA HYPOTHALAMUS; LILIUM LANCIFOLIUM BULB; MELATONIN; SUS SCROFA OVARY; SUS SCROFA PANCREAS; SUS SCROFA PINEAL GLAND; SUS SCROFA THYMUS; THYROID
Active Ingredient Strength6 [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 17089-231-18

1 BOTTLE, DROPPER in 1 BOX (17089-231-18) > 30 mL in 1 BOTTLE, DROPPER
Marketing Start Date2018-12-21
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 17089-231-18 [17089023118]

GUNA-FEM SOLUTION/ DROPS
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-12-21
Inactivation Date2020-01-31
Reactivation Date2020-03-13

Drug Details

Active Ingredients

IngredientStrength
ADENOSINE CYCLIC PHOSPHATE6 [hp_X]/30mL

OpenFDA Data

SPL SET ID:2a41728f-3270-42d7-aa4e-4c4572870d77
Manufacturer
UNII
UPC Code
  • 0317089231189
    • © 2025 FDA.report
    This site is not affiliated with or endorsed by the FDA.