Over-the-counter drug · UNAPPROVED HOMEOPATHIC
Ambrosia artemisiaefolia (Ambrosia artemisiifolia) NDC 0220-0219
Ambrosia artemisiifolia 30 [hp_C]/30[hp_C] · Pellet · Oral · Boiron
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 0220-0219-41 | 0022002194100220021941 | 30 [hp_C] in 1 TUBE (0220-0219-41)Marketed from Mar 3, 1983 | |
| 0220-0219-43 | 0022002194300220021943 | 3 TUBE in 1 PACKAGE (0220-0219-43) / 30 [hp_C] in 1 TUBEMarketed from May 11, 2020 |
How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 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)
- Ambrosia artemisiaefolia
- Generic name (nonproprietary)
- ambrosia artemisiifolia
- Active ingredients
- Ambrosia artemisiifolia — 30 [hp_C]/30[hp_C]
- Dosage form
- Pellet
- Route
- Oral
- Labeler
- BoironNDC labeler code 0220
- Product type
- Over-the-counter drug
- Marketing category
- Unapproved homeopathic
- Marketing start
- Listing expires
- Identifiers
- Product ID 0220-0219_10e04d03-329d-090f-e063-6294a90a6c72SPL ID 10e04d03-329d-090f-e063-6294a90a6c72SPL set ID 8427717f-4d1a-54b5-e053-2a91aa0a3d00UNII 9W34L2CQ9A
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
N400220021941followed by a unit qualifier and the quantityPackage 00220-0219-41. 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)
Box Purpose* Relieves symptoms of hay fever associated with ragweed allergy Tube Purpose Relieves symptoms of hay fever*
Excerpt only. Read the full label for complete information.
About NDC 0220-0219
- What is NDC 0220-0219?
- 0220-0219 is the product NDC for Ambrosia artemisiaefolia (ambrosia artemisiifolia), Ambrosia artemisiifolia 30 [hp_C]/30[hp_C] pellet, listed with the FDA by Boiron. It has 2 package NDCs, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Ambrosia artemisiaefolia (Ambrosia artemisiifolia).
- What is the active ingredient?
- Ambrosia artemisiifolia.
- Who is the labeler?
- Boiron, NDC labeler code 0220. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Ambrosia artemisiaefolia?
- 2 other product NDCs are listed under this name. See all Ambrosia artemisiaefolia NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other Ambrosia artemisiaefolia products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| Ambrosia Artemisiaefoliaambrosia artemisiifolia | Ambrosia artemisiifolia 200 [kp_C]/200[kp_C] | PelletOral | Boiron | 0220-0230 | 00220-0230-41 |
| Ambrosia artemisiaefoliaambrosia artemisiifolia | Ambrosia artemisiifolia 6 [hp_C]/6[hp_C] | PelletOral | Boiron | 0220-0218 | 00220-0218-41 |