spongia aurum (48951-8201)

Drug Facts

Product Profile

Brand Name spongia aurum

Generic Name spongia aurum

Labeler uriel pharmacy inc.

Dosage Form PELLET

Routes

ORAL

Active Ingredients

calcium carbonate 12 [hp_X]/1, gold 12 [hp_X]/1, prunus spinosa flower bud 6 [hp_X]/1, pulsatilla vulgaris 7 [hp_X]/1, sepia officinalis juice 7 [hp_X]/1, spongia officinalis skeleton, roasted 12 [hp_X]/1, sugarcane 12 [hp_X]/1

Manufacturer

Uriel Pharmacy Inc.

Identifiers & Regulatory

Product NDC 48951-8201

Product ID 48951-8201_43045028-6a29-88b4-e063-6294a90afc81

Product Type HUMAN OTC DRUG

Marketing Category UNAPPROVED HOMEOPATHIC

Listing Expiration 2026-12-31

Marketing Start 2009-09-01

Pharmacologic Class

Established (EPC)

standardized chemical allergen [epc]

Chemical Structure

allergens [cs]

Physiologic Effect

increased histamine release [pe] cell-mediated immunity [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 489518201

Hyphenated Format 48951-8201

Supplemental Identifiers

UNII

H0G9379FGK 79Y1949PYO 53Y84VPS2W I76KB35JEV QDL83WN8C2 1PIP394IID 81H2R5AOH3

NUI

N0000185508 N0000175629 N0000184306 M0000728

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 spongia aurum (source: ndc)

Generic Name spongia aurum (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

12 [hp_X]/1
6 [hp_X]/1
7 [hp_X]/1

source: ndc

Packaging

1350 PELLET in 1 BOTTLE, GLASS (48951-8201-2)

source: ndc

Packages (1)

48951-8201-2 1350 PELLET in 1 BOTTLE, GLASS (48951-8201-2)

Ingredients (7)

calcium carbonate (12 [hp_X]/1) gold (12 [hp_X]/1) prunus spinosa flower bud (6 [hp_X]/1) pulsatilla vulgaris (7 [hp_X]/1) sepia officinalis juice (7 [hp_X]/1) spongia officinalis skeleton, roasted (12 [hp_X]/1) sugarcane (12 [hp_X]/1)

Linked Drug Pages (1)

Spongia Aurum ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload

{"route": ["ORAL"], "spl_id": "43045028-6a29-88b4-e063-6294a90afc81", "openfda": {"nui": ["N0000185508", "N0000175629", "N0000184306", "M0000728"], "unii": ["H0G9379FGK", "79Y1949PYO", "53Y84VPS2W", "I76KB35JEV", "QDL83WN8C2", "1PIP394IID", "81H2R5AOH3"], "spl_set_id": ["fd805960-dfb5-4370-956a-873cf1311521"], "pharm_class_cs": ["Allergens [CS]"], "pharm_class_pe": ["Increased Histamine Release [PE]", "Cell-mediated Immunity [PE]"], "pharm_class_epc": ["Standardized Chemical Allergen [EPC]"], "manufacturer_name": ["Uriel Pharmacy Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1350 PELLET in 1 BOTTLE, GLASS (48951-8201-2)", "package_ndc": "48951-8201-2", "marketing_start_date": "20090901"}], "brand_name": "Spongia Aurum", "product_id": "48951-8201_43045028-6a29-88b4-e063-6294a90afc81", "dosage_form": "PELLET", "pharm_class": ["Allergens [CS]", "Blood Coagulation Factor [EPC]", "Calcium [CS]", "Cations", "Divalent [CS]", "Cell-mediated Immunity [PE]", "Increased Coagulation Factor Activity [PE]", "Increased Histamine Release [PE]", "Phosphate Binder [EPC]", "Phosphate Chelating Activity [MoA]", "Standardized Chemical Allergen [EPC]"], "product_ndc": "48951-8201", "generic_name": "Spongia Aurum", "labeler_name": "Uriel Pharmacy Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Spongia Aurum", "active_ingredients": [{"name": "CALCIUM CARBONATE", "strength": "12 [hp_X]/1"}, {"name": "GOLD", "strength": "12 [hp_X]/1"}, {"name": "PRUNUS SPINOSA FLOWER BUD", "strength": "6 [hp_X]/1"}, {"name": "PULSATILLA VULGARIS", "strength": "7 [hp_X]/1"}, {"name": "SEPIA OFFICINALIS JUICE", "strength": "7 [hp_X]/1"}, {"name": "SPONGIA OFFICINALIS SKELETON, ROASTED", "strength": "12 [hp_X]/1"}, {"name": "SUGARCANE", "strength": "12 [hp_X]/1"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "20090901", "listing_expiration_date": "20261231"}