natrum phosphoricum

Generic: natrum phosphoricum

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

Drug Facts

Product Profile

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

sodium phosphate, dibasic, heptahydrate 30 [hp_C]/1

Manufacturer
Hahnemann Laboratories, INC.

Identifiers & Regulatory

Product NDC 37662-1889
Product ID 37662-1889_ed01509a-afb7-476f-e053-2995a90a5aa6
Product Type HUMAN OTC DRUG
Marketing Category UNAPPROVED HOMEOPATHIC
Listing Expiration 2026-12-31
Marketing Start 2022-11-08

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 376621889
Hyphenated Format 37662-1889

Supplemental Identifiers

UNII
70WT22SF4B

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

Resolved Composition

Strengths
  • 30 [hp_C]/1
source: ndc
Packaging
  • 80 PELLET in 1 VIAL, GLASS (37662-1889-1)
  • 200 PELLET in 1 VIAL, GLASS (37662-1889-2)
  • 1200 PELLET in 1 BOTTLE, GLASS (37662-1889-3)
  • 4000 PELLET in 1 BOTTLE, GLASS (37662-1889-4)
source: ndc

Packages (4)

37662-1889-1 80 PELLET in 1 VIAL, GLASS (37662-1889-1) 37662-1889-2 200 PELLET in 1 VIAL, GLASS (37662-1889-2) 37662-1889-3 1200 PELLET in 1 BOTTLE, GLASS (37662-1889-3) 37662-1889-4 4000 PELLET in 1 BOTTLE, GLASS (37662-1889-4)

Ingredients (1)

sodium phosphate, dibasic, heptahydrate (30 [hp_C]/1)

Linked Drug Pages (1)

Natrum Phosphoricum ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "ed01509a-afb7-476f-e053-2995a90a5aa6", "openfda": {"unii": ["70WT22SF4B"], "spl_set_id": ["ed01509a-afb6-476f-e053-2995a90a5aa6"], "manufacturer_name": ["Hahnemann Laboratories, INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "80 PELLET in 1 VIAL, GLASS (37662-1889-1)", "package_ndc": "37662-1889-1", "marketing_start_date": "20221108"}, {"sample": false, "description": "200 PELLET in 1 VIAL, GLASS (37662-1889-2)", "package_ndc": "37662-1889-2", "marketing_start_date": "20221108"}, {"sample": false, "description": "1200 PELLET in 1 BOTTLE, GLASS (37662-1889-3)", "package_ndc": "37662-1889-3", "marketing_start_date": "20221108"}, {"sample": false, "description": "4000 PELLET in 1 BOTTLE, GLASS (37662-1889-4)", "package_ndc": "37662-1889-4", "marketing_start_date": "20221108"}], "brand_name": "Natrum Phosphoricum", "product_id": "37662-1889_ed01509a-afb7-476f-e053-2995a90a5aa6", "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": "37662-1889", "generic_name": "Natrum Phosphoricum", "labeler_name": "Hahnemann Laboratories, INC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Natrum Phosphoricum", "active_ingredients": [{"name": "SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE", "strength": "30 [hp_C]/1"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "20221108", "listing_expiration_date": "20261231"}