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Birch Juniper

NDC 48951-2149, Birch Juniper, liquid, from Uriel Pharmacy Inc.

Product NDC
48951-2149
Status
Listed
Labeler
Uriel Pharmacy Inc
Dosage form
LIQUID
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
UNAPPROVED HOMEOPATHIC
Application
—
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/48951-2149 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • JUNIPER BERRY1 [hp_X]/mL
  • BETULA PENDULA BARK1 [hp_X]/mL

Pharmacologic classes

Allergens [CS]; Cell-mediated Immunity [PE]; Dietary Proteins [CS]; Food Additives [CS]; Increased Histamine Release [PE]; Non-Standardized Food Allergenic Extract [EPC]; Non-Standardized Plant Allergenic Extract [EPC]; Plant Proteins [CS]

Package NDCNDC-11Package
48951-2149-948951214909240 mL in 1 BOTTLE, GLASS (48951-2149-9)

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 48951-2149 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/48951-2149 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 48951-2149. 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.