acunol

Generic: nickel sulfate, potassium bromide, sodium bromide, zinc sulfate anhydrous, and sulfur

Labeler: plymouth healthcare products llc
NDC Directory HUMAN PRESCRIPTION DRUG UNAPPROVED HOMEOPATHIC Inactive Finished

Drug Facts

Product Profile

Brand Name acunol
Generic Name nickel sulfate, potassium bromide, sodium bromide, zinc sulfate anhydrous, and sulfur
Labeler plymouth healthcare products llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

nickel sulfate 1 [hp_X]/1, potassium bromide 1 [hp_X]/1, sodium bromide 1 [hp_X]/1, sulfur 1 [hp_X]/1, zinc sulfate anhydrous 1 [hp_X]/1

Manufacturer
PLYMOUTH HEALTHCARE PRODUCTS LLC

Identifiers & Regulatory

Product NDC 61480-137
Product ID 61480-137_2b244a53-0f31-3410-e063-6394a90a06d6
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category UNAPPROVED HOMEOPATHIC
Listing Expiration 2026-12-31
Marketing Start 2006-04-18

Pharmacologic Class

Classes
copper absorption inhibitor [epc] decreased copper ion absorption [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 61480137
Hyphenated Format 61480-137

Supplemental Identifiers

UPC
0361480137052
UNII
4FLT4T3WUN OSD78555ZM LC1V549NOM 70FD1KFU70 0J6Z13X3WO

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 acunol (source: ndc)
Generic Name nickel sulfate, potassium bromide, sodium bromide, zinc sulfate anhydrous, and sulfur (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 [hp_X]/1
source: ndc
Packaging
  • 90 TABLET in 1 BOTTLE (61480-137-05)
source: ndc

Packages (1)

61480-137-05 90 TABLET in 1 BOTTLE (61480-137-05)

Ingredients (5)

nickel sulfate (1 [hp_X]/1) potassium bromide (1 [hp_X]/1) sodium bromide (1 [hp_X]/1) sulfur (1 [hp_X]/1) zinc sulfate anhydrous (1 [hp_X]/1)

Linked Drug Pages (1)

Acunol ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2b244a53-0f31-3410-e063-6394a90a06d6", "openfda": {"upc": ["0361480137052"], "unii": ["4FLT4T3WUN", "OSD78555ZM", "LC1V549NOM", "70FD1KFU70", "0J6Z13X3WO"], "spl_set_id": ["f7f1c99e-1a67-4b34-b1f4-0ac38b9d8006"], "manufacturer_name": ["PLYMOUTH HEALTHCARE PRODUCTS LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (61480-137-05)", "package_ndc": "61480-137-05", "marketing_start_date": "20060418"}], "brand_name": "Acunol", "product_id": "61480-137_2b244a53-0f31-3410-e063-6394a90a06d6", "dosage_form": "TABLET", "pharm_class": ["Copper Absorption Inhibitor [EPC]", "Decreased Copper Ion Absorption [PE]"], "product_ndc": "61480-137", "generic_name": "Nickel Sulfate, Potassium Bromide, Sodium Bromide, Zinc Sulfate Anhydrous, and Sulfur", "labeler_name": "PLYMOUTH HEALTHCARE PRODUCTS LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Acunol", "active_ingredients": [{"name": "NICKEL SULFATE", "strength": "1 [hp_X]/1"}, {"name": "POTASSIUM BROMIDE", "strength": "1 [hp_X]/1"}, {"name": "SODIUM BROMIDE", "strength": "1 [hp_X]/1"}, {"name": "SULFUR", "strength": "1 [hp_X]/1"}, {"name": "ZINC SULFATE ANHYDROUS", "strength": "1 [hp_X]/1"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "20060418", "listing_expiration_date": "20261231"}