Over-the-counter drug · UNAPPROVED HOMEOPATHIC
Plantain Beeswax NDC 48951-8419
Petasites hybridus root 4 [hp_X]/g + 4 more ingredients · Ointment · Topical · Uriel Pharmacy Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 48951-8419-5 | 4895184190548951841905 | 60 g in 1 TUBE (48951-8419-5)Marketed from Sep 1, 2009 |
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)
- Plantain Beeswax
- Generic name (nonproprietary)
- plantain beeswax
- Active ingredients
- Petasites hybridus root — 4 [hp_X]/gLarix decidua resin — 1 [hp_X]/gSage — 3 [hp_X]/gDrosera rotundifolia — 4 [hp_X]/gPlantago major leaf — 4 [hp_X]/g
- Dosage form
- Ointment
- Route
- Topical
- Labeler
- Uriel Pharmacy Inc.NDC labeler code 48951
- Product type
- Over-the-counter drug
- Marketing category
- Unapproved homeopathic
- Marketing start
- Listing expires
- Other FDA classes
- Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Dietary Proteins (Chemical structure)Increased Histamine Release (Physiologic effect)Plant Proteins (Chemical structure)
- Identifiers
- Product ID 48951-8419_2b247033-d7c4-61c6-e063-6394a90a48f6SPL ID 2b247033-d7c4-61c6-e063-6394a90a48f6SPL set ID 26facd12-ab50-e2c4-e063-6394a90ae8d1UNII 97S2809V5R, AD8LJ73GQF, 065C5D077J, QR44N9XPJQ, 7DC28K241X
- Pharmacologic class
- Non-Standardized Food Allergenic Extract; Non-Standardized Plant Allergenic Extract
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. Topical products like this are usually dispensed by a pharmacy and billed by NDC.
- NDC on a medical claim
N448951841905followed by a unit qualifier and the quantityPackage 48951-8419-05. 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)
Directions: FOR TOPICAL USE ONLY.
Excerpt only. Read the full label for complete information.
About NDC 48951-8419
- What is NDC 48951-8419?
- 48951-8419 is the product NDC for Plantain Beeswax, Petasites hybridus root 4 [hp_X]/g + 4 more ingredients ointment, listed with the FDA by Uriel Pharmacy Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Plantain Beeswax.
- What is the active ingredient?
- Petasites hybridus root, Larix decidua resin, Sage, Drosera rotundifolia, Plantago major leaf.
- Who is the labeler?
- Uriel Pharmacy Inc., NDC labeler code 48951. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Plantain Beeswax?
- 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.