Prescription drug · UNAPPROVED HOMEOPATHIC
Acunol NDC 61480-137
Nickel sulfate 1 [hp_X]/1 + 4 more ingredients · Tablet · Oral · PLYMOUTH HEALTHCARE PRODUCTS LLC
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 61480-137-05 | 6148001370561480013705 | 90 TABLET in 1 BOTTLE (61480-137-05)Marketed from Apr 18, 2006 |
How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules
Product information
- Brand name (proprietary)
- Acunol
- Generic name (nonproprietary)
- nickel sulfate, potassium bromide, sodium bromide, zinc sulfate anhydrous, and sulfur
- Active ingredients
- Nickel sulfate — 1 [hp_X]/1Potassium bromide — 1 [hp_X]/1Sodium bromide — 1 [hp_X]/1Zinc sulfate anhydrous — 1 [hp_X]/1Sulfur — 1 [hp_X]/1
- Dosage form
- Tablet
- Route
- Oral
- Labeler
- PLYMOUTH HEALTHCARE PRODUCTS LLCNDC labeler code 61480
- Product type
- Prescription drug
- Marketing category
- Unapproved homeopathic
- Marketing start
- Listing expires
- Other FDA classes
- Decreased Copper Ion Absorption (Physiologic effect)
- Identifiers
- Product ID 61480-137_2b244a53-0f31-3410-e063-6394a90a06d6SPL ID 2b244a53-0f31-3410-e063-6394a90a06d6SPL set ID f7f1c99e-1a67-4b34-b1f4-0ac38b9d8006UNII 4FLT4T3WUN, OSD78555ZM, LC1V549NOM, 0J6Z13X3WO, 70FD1KFU70UPC 0361480137052
- Pharmacologic class
- Copper Absorption Inhibitor
Billing references
What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.
- HCPCS codeNo match
No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.
- NDC on a medical claim
N461480013705followed by a unit qualifier and the quantityPackage 61480-0137-05. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier
Product label
Current FDA label (SPL), effective .
Indications (excerpt from the label)
INDICATIONS Acunol™ is indicated for the treatment of mild to moderate acne vulgaris, acne rosacea, peri-oral dermatitis, and folliculitis. It has been found to work well with a variety of combination therapies.
Excerpt only. Read the full label for complete information.
About NDC 61480-137
- What is NDC 61480-137?
- 61480-137 is the product NDC for Acunol, Nickel sulfate 1 [hp_X]/1 + 4 more ingredients tablet, listed with the FDA by PLYMOUTH HEALTHCARE PRODUCTS LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Acunol (Nickel Sulfate, Potassium Bromide, Sodium Bromide, Zinc Sulfate Anhydrous, and Sulfur).
- What is the active ingredient?
- Nickel sulfate, Potassium bromide, Sodium bromide, Zinc sulfate anhydrous, Sulfur.
- Who is the labeler?
- PLYMOUTH HEALTHCARE PRODUCTS LLC, NDC labeler code 61480. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Acunol?
- None: this is the only finished product listed under this name.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.