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Polygonatum Cepa

NDC 48951-8310, Polygonatum Cepa, gel, from Uriel Pharmacy Inc..

Product NDC
48951-8310
Status
Listed
Labeler
Uriel Pharmacy Inc.
Dosage form
GEL
Route
TOPICAL
Product type
HUMAN OTC DRUG
Marketing category
UNAPPROVED HOMEOPATHIC
Application
—
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/48951-8310 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ONION2 [hp_X]/g
  • ECHINACEA ANGUSTIFOLIA2 [hp_X]/g
  • HIRUDIN4 [hp_X]/g
  • POLYGONATUM CYRTONEMA ROOT4 [hp_X]/g
  • VESPA CRABRO6 [hp_X]/g
  • GOLD8 [hp_X]/g
  • BOS TAURUS CARTILAGE8 [hp_X]/g
  • COPPER8 [hp_X]/g
  • SUS SCROFA SKIN8 [hp_X]/g
  • BOS TAURUS PLACENTA8 [hp_X]/g
  • SILICON DIOXIDE8 [hp_X]/g
  • THUJA OCCIDENTALIS WHOLE8 [hp_X]/g
  • SILVER12 [hp_X]/g
  • BARIUM CITRATE12 [hp_X]/g
  • GRAPHITE17 [hp_X]/g

Pharmacologic classes

Allergens [CS]; Allergens [CS]; Allergens [CS]; Cell-mediated Immunity [PE]; Cell-mediated Immunity [PE]; Cell-mediated Immunity [PE]; Cells, Epidermal [EXT]; Copper [CS]; Copper-containing Intrauterine Device [EPC]; Decreased Embryonic Implantation [PE]; Decreased Sperm Motility [PE]; Dietary Proteins [CS]; Increased Histamine Release [PE]; Increased Histamine Release [PE]; Increased Histamine Release [PE]; Increased IgG Production [PE]; Inhibit Ovum Fertilization [PE]; Non-Standardized Animal Skin Allergenic Extract [EPC]; Non-Standardized Food Allergenic Extract [EPC]; Standardized Chemical Allergen [EPC]; Vegetable Proteins [CS]

Package NDCNDC-11Package
48951-8310-54895183100560 g in 1 TUBE (48951-8310-5)

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 48951-8310 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/48951-8310 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 48951-8310. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.