gentiana absinthium

Generic: gentiana absinthium

Labeler: uriel pharmacy inc.
NDC Directory HUMAN OTC DRUG UNAPPROVED HOMEOPATHIC Inactive Finished

Drug Facts

Product Profile

Brand Name gentiana absinthium
Generic Name gentiana absinthium
Labeler uriel pharmacy inc.
Dosage Form LIQUID
Routes
ORAL
Active Ingredients

gentiana lutea root 3 [hp_X]/mL, strychnos nux-vomica seed 6 [hp_X]/mL, taraxacum palustre root 3 [hp_X]/mL, wormwood 3 [hp_X]/mL

Manufacturer
Uriel Pharmacy Inc.

Identifiers & Regulatory

Product NDC 48951-5007
Product ID 48951-5007_2b250370-261d-fe8f-e063-6394a90a6423
Product Type HUMAN OTC DRUG
Marketing Category UNAPPROVED HOMEOPATHIC
Listing Expiration 2026-12-31
Marketing Start 2009-09-01

Pharmacologic Class

Established (EPC)
non-standardized plant allergenic extract [epc]
Chemical Structure
allergens [cs] plant proteins [cs] seed storage proteins [cs]
Physiologic Effect
increased histamine release [pe] cell-mediated immunity [pe] increased igg production [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 489515007
Hyphenated Format 48951-5007

Supplemental Identifiers

UNII
S72O3284MS 269XH13919 GCZ4W7077C F84709P2XV
NUI
N0000185375 N0000175629 N0000184306 N0000185001 M0000728 M0016962 M0516536

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name gentiana absinthium (source: ndc)
Generic Name gentiana absinthium (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 3 [hp_X]/mL
  • 6 [hp_X]/mL
source: ndc
Packaging
  • 10 AMPULE in 1 BOX (48951-5007-1) / 1 mL in 1 AMPULE
source: ndc

Packages (1)

48951-5007-1 10 AMPULE in 1 BOX (48951-5007-1) / 1 mL in 1 AMPULE

Ingredients (4)

gentiana lutea root (3 [hp_X]/mL) strychnos nux-vomica seed (6 [hp_X]/mL) taraxacum palustre root (3 [hp_X]/mL) wormwood (3 [hp_X]/mL)

Linked Drug Pages (1)

Gentiana Absinthium ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2b250370-261d-fe8f-e063-6394a90a6423", "openfda": {"nui": ["N0000185375", "N0000175629", "N0000184306", "N0000185001", "M0000728", "M0016962", "M0516536"], "unii": ["S72O3284MS", "269XH13919", "GCZ4W7077C", "F84709P2XV"], "spl_set_id": ["1b53081c-717e-46ae-8f86-e6f070c3c97d"], "pharm_class_cs": ["Allergens [CS]", "Plant Proteins [CS]", "Seed Storage Proteins [CS]"], "pharm_class_pe": ["Increased Histamine Release [PE]", "Cell-mediated Immunity [PE]", "Increased IgG Production [PE]"], "pharm_class_epc": ["Non-Standardized Plant Allergenic Extract [EPC]"], "manufacturer_name": ["Uriel Pharmacy Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 AMPULE in 1 BOX (48951-5007-1)  / 1 mL in 1 AMPULE", "package_ndc": "48951-5007-1", "marketing_start_date": "20090901"}], "brand_name": "Gentiana Absinthium", "product_id": "48951-5007_2b250370-261d-fe8f-e063-6394a90a6423", "dosage_form": "LIQUID", "pharm_class": ["Allergens [CS]", "Cell-mediated Immunity [PE]", "Increased Histamine Release [PE]", "Increased IgG Production [PE]", "Non-Standardized Plant Allergenic Extract [EPC]", "Plant Proteins [CS]", "Seed Storage Proteins [CS]"], "product_ndc": "48951-5007", "generic_name": "Gentiana Absinthium", "labeler_name": "Uriel Pharmacy Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Gentiana Absinthium", "active_ingredients": [{"name": "GENTIANA LUTEA ROOT", "strength": "3 [hp_X]/mL"}, {"name": "STRYCHNOS NUX-VOMICA SEED", "strength": "6 [hp_X]/mL"}, {"name": "TARAXACUM PALUSTRE ROOT", "strength": "3 [hp_X]/mL"}, {"name": "WORMWOOD", "strength": "3 [hp_X]/mL"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "20090901", "listing_expiration_date": "20261231"}