spongilla lacustris mt

Generic: spongilla lacustris

Labeler: ohm pharma inc.
NDC Directory HUMAN PRESCRIPTION DRUG UNAPPROVED HOMEOPATHIC Inactive Finished

Drug Facts

Product Profile

Brand Name spongilla lacustris mt
Generic Name spongilla lacustris
Labeler ohm pharma inc.
Dosage Form TINCTURE
Routes
ORAL
Active Ingredients

spongilla lacustris 1 [hp_X]/.25L

Manufacturer
OHM PHARMA INC.

Identifiers & Regulatory

Product NDC 66096-749
Product ID 66096-749_d449d3d9-49bd-2a4b-e053-2995a90a5a95
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category UNAPPROVED HOMEOPATHIC
Listing Expiration 2026-12-31
Marketing Start 2019-03-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 66096749
Hyphenated Format 66096-749

Supplemental Identifiers

UNII
6SZ0G98BHM

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 spongilla lacustris mt (source: ndc)
Generic Name spongilla lacustris (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 [hp_X]/.25L
source: ndc
Packaging
  • .25 L in 1 BOTTLE (66096-749-08)
source: ndc

Packages (1)

66096-749-08 .25 L in 1 BOTTLE (66096-749-08)

Ingredients (1)

spongilla lacustris (1 [hp_X]/.25L)

Linked Drug Pages (1)

Spongilla lacustris MT ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "d449d3d9-49bd-2a4b-e053-2995a90a5a95", "openfda": {"unii": ["6SZ0G98BHM"], "spl_set_id": ["a855d4ca-52ed-4e69-93b5-7304bcc84f73"], "manufacturer_name": ["OHM PHARMA INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": ".25 L in 1 BOTTLE (66096-749-08)", "package_ndc": "66096-749-08", "marketing_start_date": "20190301"}], "brand_name": "Spongilla lacustris MT", "product_id": "66096-749_d449d3d9-49bd-2a4b-e053-2995a90a5a95", "dosage_form": "TINCTURE", "product_ndc": "66096-749", "generic_name": "Spongilla lacustris", "labeler_name": "OHM PHARMA INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Spongilla lacustris MT", "active_ingredients": [{"name": "SPONGILLA LACUSTRIS", "strength": "1 [hp_X]/.25L"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "20190301", "listing_expiration_date": "20261231"}