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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
Request
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 NDCNDC-11Package
17089-501-18170890501181 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
curl https://api.healthcare.dev/v1/drugs/ndc/17089-501 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
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.