United States · FDA National Drug Code directory
Borago Nicotiana
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 48951-2077_53872d71-7ff6-38cc-e063-6294a90a9913
- Product NDC
- 48951-2077
- Form
- LIQUID
- Composition / generic term
- Borago Nicotiana
- Labeler
- Uriel Pharmacy Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start / end (source format)
- 20090901
- Source listing expiry
- 20271231
Source-listed ingredients
- BORAGE — 3 [hp_X]/mL
- CENTAUREA BENEDICTA — 3 [hp_X]/mL
- HAMAMELIS VIRGINIANA LEAF — 3 [hp_X]/mL
- TOBACCO LEAF — 6 [hp_X]/mL
- ALUMINUM OXIDE — 8 [hp_X]/mL
- FERROUS ARSENATE — 10 [hp_X]/mL
- HORSE CHESTNUT — 10 [hp_X]/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 10 AMPULE in 1 BOX (48951-2077-1) / 1 mL in 1 AMPULE · 48951-2077-1
Source and coverage
Open FDA National Drug Code directory →
Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
Browse United States records →