NDC codes

FDA NDC Directory
Product NDC (as listed)42681-9033Labeler and product segments. Claims need a package NDC.
Product NDC at billing width42681-9033Add 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
42681-9033-24268190330242681903302200 mL in 1 BOTTLE (42681-9033-2)Marketed from Jan 3, 2011

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

Generic name (nonproprietary)
antimony potassium tartrate, bryonia alba root, protortonia cacti, drosera rotundifolia, ipecac, pulsatilla vulgaris, rumex crispus root, pongia officinalis skeleton, roasted, lobaria pulmonaria
Active ingredients
Bryonia alba root — 3 [hp_C]/mLProtortonia cacti — 3 [hp_C]/mLDrosera rotundifolia — 3 [hp_C]/mLIpecac — 3 [hp_C]/mLPulsatilla vulgaris — 6 [hp_C]/mLRumex crispus root — 6 [hp_C]/mLSpongia officinalis skeleton, Roasted — 3 [hp_C]/mLLobaria pulmonaria — 3 [hp_C]/mLAntimony potassium tartrate — 6 [hp_C]/mL
Dosage form
Syrup
Route
Oral
Labeler
WFM Private Label, LPNDC labeler code 42681
Product type
Over-the-counter drug
Marketing category
Unapproved homeopathic
Marketing start
Listing expires
Identifiers
Product ID 42681-9033_06eae910-1e66-71c8-e063-6294a90a91ccSPL ID 06eae910-1e66-71c8-e063-6294a90a91ccSPL set ID 5abb1868-2539-4078-8e86-11879fafa633UNII T7J046YI2B, LZB7TFX1LT, QR44N9XPJQ, 62I3C8233L, I76KB35JEV, 9N1RM2S62C, 1PIP394IID, D1YM0P5Z2T, DL6OZ476V3

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

N442681903302 followed by a unit qualifier and the quantity

Package 42681-9033-02. 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)

Temporary relieves cough due to minor throat and bronchial irritation as may occur with a cold. Helps loosen phlegms (mucus) and thin bronchial secretions to make coughs more productive.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 42681-9033

What is NDC 42681-9033?
42681-9033 is the product NDC for 365 Everyday Value Be Well Cough Ease for Kids, Bryonia alba root 3 [hp_C]/mL + 8 more ingredients syrup, listed with the FDA by WFM Private Label, LP. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
365 Everyday Value Be Well Cough Ease for Kids (Antimony potassium tartrate, Bryonia alba root, Protortonia cacti, Drosera rotundifolia, Ipecac, Pulsatilla vulgaris, Rumex crispus root, Pongia officinalis skeleton, Roasted, Lobaria pulmonaria).
What is the active ingredient?
Bryonia alba root, Protortonia cacti, Drosera rotundifolia, Ipecac, Pulsatilla vulgaris, Rumex crispus root, Spongia officinalis skeleton, Roasted, Lobaria pulmonaria, Antimony potassium tartrate.
Who is the labeler?
WFM Private Label, LP, NDC labeler code 42681. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for 365 Everyday Value Be Well Cough Ease for Kids?
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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