GUNA FEMALE SUPPORT
NDC 17089-501, lilium lancifolium whole flowering - sus scrofa ovary - sus scrofa pituitary gland - sepia officinalis juice - adenosine cyclic phosphate - pulsatilla vulgaris - sus scrofa hypothalamus - sus scrofa adrenal gland - sus scrofa pancreas - magnesium phosphate dibasic trihydrate, solution/ drops, from Guna spa.
- Product NDC
- 17089-501
- Status
- Listed
- Labeler
- Guna spa
- Dosage form
- SOLUTION/ DROPS
- Route
- ORAL
- Product type
- HUMAN OTC DRUG
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Application
- —
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/17089-501 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- LILIUM LANCIFOLIUM WHOLE FLOWERING6 [hp_X]/30mL
- SUS SCROFA OVARY6 [hp_X]/30mL
- SEPIA OFFICINALIS JUICE10 [hp_X]/30mL
- ADENOSINE CYCLIC PHOSPHATE6 [hp_X]/30mL
- SUS SCROFA PITUITARY GLAND30 [hp_X]/30mL
- SUS SCROFA HYPOTHALAMUS30 [hp_X]/30mL
- SUS SCROFA ADRENAL GLAND30 [hp_X]/30mL
- SUS SCROFA PANCREAS30 [hp_X]/30mL
- MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE10 [hp_X]/30mL
- PULSATILLA VULGARIS8 [hp_X]/30mL
Pharmacologic classes
Calculi Dissolution Agent [EPC]; Increased Large Intestinal Motility [PE]; Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]; Inhibition Small Intestine Fluid/Electrolyte Absorption [PE]; Magnesium Ion Exchange Activity [MoA]; Osmotic Activity [MoA]; Osmotic Laxative [EPC]; Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 17089-501-18 | 17089050118 | 1 BOTTLE, DROPPER in 1 BOX (17089-501-18) / 30 mL in 1 BOTTLE, DROPPER |
Linked data
RxNorm, label and prices
RxNorm concepts
RxNorm links no concept to this product's packages.
Related lookups
No FDA label, Medicare Part B payment limit or NADAC price is linked to this product.
Use it
Look up 17089-501 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/17089-501 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 17089-501. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.