natrum oxydatum

Generic: natrum oxydatum

Labeler: hahnemann laboratories, inc.
NDC Directory HUMAN OTC DRUG UNAPPROVED HOMEOPATHIC Inactive Finished

Drug Facts

Product Profile

Brand Name natrum oxydatum
Generic Name natrum oxydatum
Labeler hahnemann laboratories, inc.
Dosage Form PELLET
Routes
ORAL
Active Ingredients

sodium oxide 30 [hp_C]/1

Manufacturer
Hahnemann Laboratories, INC.

Identifiers & Regulatory

Product NDC 37662-3850
Product ID 37662-3850_0416ce03-c344-9d9e-e063-6294a90ad940
Product Type HUMAN OTC DRUG
Marketing Category UNAPPROVED HOMEOPATHIC
Listing Expiration 2026-12-31
Marketing Start 2023-08-29

Pharmacologic Class

Classes
increased large intestinal motility [pe] inhibition large intestine fluid/electrolyte absorption [pe] osmotic activity [moa] osmotic laxative [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 376623850
Hyphenated Format 37662-3850

Supplemental Identifiers

UNII
3075U8R23D

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 natrum oxydatum (source: ndc)
Generic Name natrum oxydatum (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 30 [hp_C]/1
source: ndc
Packaging
  • 80 PELLET in 1 VIAL, GLASS (37662-3850-1)
  • 200 PELLET in 1 VIAL, GLASS (37662-3850-2)
  • 1200 PELLET in 1 BOTTLE, GLASS (37662-3850-3)
  • 4000 PELLET in 1 BOTTLE, GLASS (37662-3850-4)
source: ndc

Packages (4)

Ingredients (1)

sodium oxide (30 [hp_C]/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0416ce03-c344-9d9e-e063-6294a90ad940", "openfda": {"unii": ["3075U8R23D"], "spl_set_id": ["0416ce03-c343-9d9e-e063-6294a90ad940"], "manufacturer_name": ["Hahnemann Laboratories, INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "80 PELLET in 1 VIAL, GLASS (37662-3850-1)", "package_ndc": "37662-3850-1", "marketing_start_date": "20230829"}, {"sample": false, "description": "200 PELLET in 1 VIAL, GLASS (37662-3850-2)", "package_ndc": "37662-3850-2", "marketing_start_date": "20230829"}, {"sample": false, "description": "1200 PELLET in 1 BOTTLE, GLASS (37662-3850-3)", "package_ndc": "37662-3850-3", "marketing_start_date": "20230829"}, {"sample": false, "description": "4000 PELLET in 1 BOTTLE, GLASS (37662-3850-4)", "package_ndc": "37662-3850-4", "marketing_start_date": "20230829"}], "brand_name": "Natrum Oxydatum", "product_id": "37662-3850_0416ce03-c344-9d9e-e063-6294a90ad940", "dosage_form": "PELLET", "pharm_class": ["Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]"], "product_ndc": "37662-3850", "generic_name": "Natrum Oxydatum", "labeler_name": "Hahnemann Laboratories, INC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Natrum Oxydatum", "active_ingredients": [{"name": "SODIUM OXIDE", "strength": "30 [hp_C]/1"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "20230829", "listing_expiration_date": "20261231"}