What is NDC 66096-708?

66096-708 is the product NDC for Kids Cough Relief Syrup, Antimony pentasulfide 12 [hp_X]/148mL + 8 more ingredients liquid, 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?

Kids Cough Relief Syrup (Antimonium Sulphuratum Aureum, Antimonium Tartaricum, Bryonia Alba, Drosera Rotundifolia, Ipecacuanha, Kali Muriaticum, Rumex Crispus, Senega Officinalis, Spongia Tosta.).

What is the active ingredient?

Antimony pentasulfide, Antimony potassium tartrate, Bryonia alba root, Drosera rotundifolia, Ipecac, Potassium chloride, Rumex crispus root, Polygala senega root, Spongia officinalis skeleton, Roasted.

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 Kids Cough Relief Syrup?

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.

Kids Cough Relief Syrup NDC 66096-708 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)66096-708Labeler and product segments. Claims need a package NDC.

Product NDC at billing width66096-0708Add 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
66096-708-25	66096070825	148 mL in 1 BOTTLE (66096-708-25)Marketed from Aug 20, 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): Kids Cough Relief Syrup
Generic name (nonproprietary): antimonium sulphuratum aureum, antimonium tartaricum, bryonia alba, drosera rotundifolia, ipecacuanha, kali muriaticum, rumex crispus, senega officinalis, spongia tosta.
Active ingredients: Antimony pentasulfide — 12 [hp_X]/148mLAntimony potassium tartrate — 6 [hp_X]/148mLBryonia alba root — 6 [hp_X]/148mLDrosera rotundifolia — 6 [hp_X]/148mLIpecac — 6 [hp_X]/148mLPotassium chloride — 6 [hp_X]/148mLRumex crispus root — 6 [hp_X]/148mLPolygala senega root — 6 [hp_X]/148mLSpongia officinalis skeleton, Roasted — 6 [hp_X]/148mL
Dosage form: Liquid
Route: Oral
Labeler: OHM PHARMA INC.NDC labeler code 66096
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Aug 20, 2015
Listing expires: Dec 31, 2026
Other FDA classes: Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Osmotic Activity (Mechanism)Potassium Compounds (Chemical structure)
Identifiers: Product ID 66096-708_d44b323b-0816-b3d4-e053-2995a90aafb7SPL ID d44b323b-0816-b3d4-e053-2995a90aafb7SPL set ID b09a9fbc-15ad-4c60-bce8-e1097d241f2cUNII 1433F1I86N, DL6OZ476V3, T7J046YI2B, QR44N9XPJQ, 62I3C8233L, 660YQ98I10, 9N1RM2S62C, M7T6H7D4IF, 1PIP394IIDUPC 0366096708252
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

N466096070825 followed by a unit qualifier and the quantity

Package 66096-0708-25. 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 Dec 29, 2021.

Indications (excerpt from the label)

USES: Temporarily relieves cough symptoms of diverse origins. Loosens chest congestion facilitating a productive cough. Soothes dry cough due to throat and bronquial irritation.** **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 66096-708

What is NDC 66096-708?: 66096-708 is the product NDC for Kids Cough Relief Syrup, Antimony pentasulfide 12 [hp_X]/148mL + 8 more ingredients liquid, 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?: Kids Cough Relief Syrup (Antimonium Sulphuratum Aureum, Antimonium Tartaricum, Bryonia Alba, Drosera Rotundifolia, Ipecacuanha, Kali Muriaticum, Rumex Crispus, Senega Officinalis, Spongia Tosta.).
What is the active ingredient?: Antimony pentasulfide, Antimony potassium tartrate, Bryonia alba root, Drosera rotundifolia, Ipecac, Potassium chloride, Rumex crispus root, Polygala senega root, Spongia officinalis skeleton, Roasted.
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 Kids Cough Relief Syrup?: 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.