What is NDC 66096-706?

66096-706 is the product NDC for OHM Mucus Relief, Antimony trisulfide 6 [hp_C]/1 + 8 more ingredients tablet, chewable, listed with the FDA by OHM PHARMA INC.. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

OHM Mucus Relief (Antimonium Crudum, Antimonium Tartaricum, Chelidonium Majus, Ferrum Phosphoricum, Kali Carboonicum, Kali muriaticum, Kali Sulphuricum, Marrubium Vulgare.).

What is the active ingredient?

Antimony trisulfide, Antimony potassium tartrate, Chelidonium majus, Ferrosoferric phosphate, Potassium dichromate, Potassium carbonate, Potassium chloride, Potassium sulfate, Marrubium vulgare.

OHM PHARMA INC., NDC labeler code 66096. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for OHM Mucus Relief?

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.

OHM Mucus Relief NDC 66096-706 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)66096-706Labeler and product segments. Claims need a package NDC.

Product NDC at billing width66096-0706Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
66096-706-23	6609607062366096070623	186 TABLET, CHEWABLE in 1 BOTTLE (66096-706-23)Marketed from May 14, 2015

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): OHM Mucus Relief
Generic name (nonproprietary): antimonium crudum, antimonium tartaricum, chelidonium majus, ferrum phosphoricum, kali carboonicum, kali muriaticum, kali sulphuricum, marrubium vulgare.
Active ingredients: Antimony trisulfide — 6 [hp_C]/1Antimony potassium tartrate — 6 [hp_C]/1Chelidonium majus — 6 [hp_X]/1Ferrosoferric phosphate — 6 [hp_X]/1Potassium dichromate — 12 [hp_X]/1Potassium carbonate — 30 [hp_C]/1Potassium chloride — 6 [hp_X]/1Potassium sulfate — 6 [hp_X]/1Marrubium vulgare — 9 [hp_C]/1
Dosage form: Tablet, Chewable
Route: Oral
Labeler: OHM PHARMA INC.NDC labeler code 66096
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: May 14, 2015
Listing expires: Dec 31, 2026
Other FDA classes: Increased Large Intestinal Motility (Physiologic effect)Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Osmotic Activity (Mechanism)Osmotic Activity (Mechanism)Potassium Compounds (Chemical structure)Potassium Compounds (Chemical structure)
Identifiers: Product ID 66096-706_b8a719c7-3b71-773b-e053-2995a90af29bSPL ID b8a719c7-3b71-773b-e053-2995a90af29bSPL set ID f13bff50-7087-46dc-a958-b460a2af6283UNII F79059A38U, DL6OZ476V3, 7E889U5RNN, 91GQH8I5F7, T4423S18FM, BQN1B9B9HA, 660YQ98I10, 1K573LC5TV, 7A72MUN24ZUPC 0366096706234
Pharmacologic class: Osmotic Laxative; Potassium Salt

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

N466096070623 followed by a unit qualifier and the quantity

Package 66096-0706-23. 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 Jan 11, 2021.

Indications (excerpt from the label)

USES: Temporarily relieves mucus and phlegm, congestion in throat.** **This statement has not been evaluated by the FDA. It is based on documented Homeopathic Materia Medica.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 66096-706

What is NDC 66096-706?: 66096-706 is the product NDC for OHM Mucus Relief, Antimony trisulfide 6 [hp_C]/1 + 8 more ingredients tablet, chewable, listed with the FDA by OHM PHARMA INC.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: OHM Mucus Relief (Antimonium Crudum, Antimonium Tartaricum, Chelidonium Majus, Ferrum Phosphoricum, Kali Carboonicum, Kali muriaticum, Kali Sulphuricum, Marrubium Vulgare.).
What is the active ingredient?: Antimony trisulfide, Antimony potassium tartrate, Chelidonium majus, Ferrosoferric phosphate, Potassium dichromate, Potassium carbonate, Potassium chloride, Potassium sulfate, Marrubium vulgare.
Who is the labeler?: OHM PHARMA INC., NDC labeler code 66096. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for OHM Mucus Relief?: 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.