NDC codes

FDA NDC Directory
Product NDC (as listed)49035-925Labeler and product segments. Claims need a package NDC.
Product NDC at billing width49035-0925Add 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
49035-925-0149035092501490350925011 KIT in 1 CARTON (49035-925-01) * 118 mL in 1 BOTTLE, PLASTIC (49035-920-01) * 1 BOTTLE, PLASTIC in 1 CARTON (49035-927-01) / 118 mL in 1 BOTTLE, PLASTICMarketed from Jul 1, 2018

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

Generic name (nonproprietary)
onion,matricaria chamomilla,arabica coffee bean,calcium sulfide,goldenseal,sodium chloride,phosphorus,anemone pulsatilla and sulfur
Dosage form
Kit
Labeler
Wal-Mart Stores, IncNDC labeler code 49035
Product type
Over-the-counter drug
Marketing category
Unapproved homeopathic
Marketing start
Listing expires
Identifiers
Product ID 49035-925_4651c400-1954-9ba4-e063-6294a90a8532SPL ID 4651c400-1954-9ba4-e063-6294a90a8532SPL set ID 70454f5a-b5ca-8d30-e053-2991aa0a1afc

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 drug-specific HCPCS code in Med-Code's directory for this product. The directory is curated and not complete — check the current CMS HCPCS file before billing.

NDC on a medical claim

N449035092501 followed by a unit qualifier and the quantity

Package 49035-0925-01. 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 Temporarily relieves the symptoms of the common cold including nasal and chest congestion, runny nose, sore throat, sneezing and cough.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 49035-925

What is NDC 49035-925?
49035-925 is the product NDC for Childrens Cold and Cough Day and Night Twin Pack kit, listed with the FDA by Wal-Mart Stores, Inc. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Childrens Cold and Cough Day and Night Twin Pack (ONION,MATRICARIA CHAMOMILLA,ARABICA COFFEE BEAN,CALCIUM SULFIDE,GOLDENSEAL,SODIUM CHLORIDE,PHOSPHORUS,ANEMONE PULSATILLA and SULFUR).
Who is the labeler?
Wal-Mart Stores, Inc, NDC labeler code 49035. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Childrens Cold and Cough Day and Night Twin Pack?
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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