NDC codes

FDA NDC Directory
Product NDC (as listed)11822-1181Labeler and product segments. Claims need a package NDC.
Product NDC at billing width11822-1181Add 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 NDC11-digit (billing)PackageCopy
11822-1181-8118221181081182211810818 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (11822-1181-8)Marketed from Apr 15, 2020

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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)
Rite Aid Ultra Zinc Cold Therapy
Generic name (nonproprietary)
zincum gluconicum
Active ingredients
Zinc gluconate — 1 [hp_X]/1
Dosage form
Tablet, Chewable
Route
Oral
Labeler
RITE AID CORPORATIONNDC labeler code 11822
Product type
Over-the-counter drug
Marketing category
Unapproved homeopathic
Marketing start
Listing expires
Other FDA classes
Decreased Copper Ion Absorption (Physiologic effect)
Identifiers
Product ID 11822-1181_8f5a0df2-6381-4b78-9ebd-20e2c30c1c0bSPL ID 8f5a0df2-6381-4b78-9ebd-20e2c30c1c0bSPL set ID ecd80b14-bf51-4e71-83bc-169864b6884dUNII U6WSN5SQ1Z
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

N411822118108 followed by a unit qualifier and the quantity

Package 11822-1181-08. 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)

Uses ▪ may help reduce duration of cold symptoms: ▪ sore throat ▪ stuffy nose ▪ sneezing ▪ coughing This product was formulated to help reduce the duration and severity of cold symptoms and was not formulated to be effective for flu or allergies. Warnings Ask a doctor before use if you have ▪ a sensitivity to zinc or are allergic zinc ▪ are taking minocycline, doxycycline, tetracycline or are on Coumadin therapy, zinc treatment may inhibit the absorption of these medicines. Stop Use and ask a doctor If symptoms persist beyond 7 days. If pregnant or breast feeding ask health professional before use. Keep Out of Reach of Children In case of overdose, get medical help or contact a Poison Contro…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 11822-1181

What is NDC 11822-1181?
11822-1181 is the product NDC for Rite Aid Ultra Zinc Cold Therapy (zincum gluconicum), Zinc gluconate 1 [hp_X]/1 tablet, chewable, listed with the FDA by RITE AID CORPORATION. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Rite Aid Ultra Zinc Cold Therapy (Zincum Gluconicum).
What is the active ingredient?
Zinc gluconate.
Who is the labeler?
RITE AID CORPORATION, NDC labeler code 11822. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Rite Aid Ultra Zinc Cold Therapy?
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.

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