United States · FDA National Drug Code directory

Acunol

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
61480-137_2b244a53-0f31-3410-e063-6394a90a06d6
Product NDC
61480-137
Form
TABLET
Composition / generic term
Nickel Sulfate, Potassium Bromide, Sodium Bromide, Zinc Sulfate Anhydrous, and Sulfur
Labeler
PLYMOUTH HEALTHCARE PRODUCTS LLC
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start / end (source format)
20060418
Source listing expiry
20261231

Source-listed ingredients

  • NICKEL SULFATE — 1 [hp_X]/1
  • POTASSIUM BROMIDE — 1 [hp_X]/1
  • SODIUM BROMIDE — 1 [hp_X]/1
  • ZINC SULFATE ANHYDROUS — 1 [hp_X]/1
  • SULFUR — 1 [hp_X]/1

These values do not establish equivalence or a dose recommendation.

Packages

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

Source and coverage

Open FDA National Drug Code directory

Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

Browse United States records →