Over-the-counter drug · UNAPPROVED HOMEOPATHIC
Rhus Aconitum NDC 48951-8140
Gelsemium sempervirens root 4 [hp_X]/mL + 6 more ingredients · Liquid · Oral · Uriel Pharmacy Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 48951-8140-1 | 4895181400148951814001 | 10 AMPULE in 1 BOX (48951-8140-1) / 1 mL in 1 AMPULEMarketed 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)
- Rhus Aconitum
- Generic name (nonproprietary)
- rhus aconitum
- Active ingredients
- Gelsemium sempervirens root — 4 [hp_X]/mLPseudognaphalium luteoalbum leaf — 4 [hp_X]/mLAconitum napellus — 6 [hp_X]/mLAtropa belladonna — 6 [hp_X]/mLMandragora officinarum root — 6 [hp_X]/mLToxicodendron pubescens leaf — 6 [hp_X]/mLPenoxsulam — 10 [hp_X]/mL
- Dosage form
- Liquid
- Route
- Oral
- Labeler
- Uriel Pharmacy Inc.NDC labeler code 48951
- Product type
- Over-the-counter drug
- Marketing category
- Unapproved homeopathic
- Marketing start
- Listing expires
- Identifiers
- Product ID 48951-8140_4bd37192-f7e8-b961-e063-6294a90ab3d3SPL ID 4bd37192-f7e8-b961-e063-6294a90ab3d3SPL set ID a176c241-fc2d-4fea-82d9-81183971b4cfUNII 639KR60Q1Q, BGI20Z6M57, U0NQ8555JD, WQZ3G9PF0H, I2XCB174VB, 6IO182RP7A, 784ELC1SCZ
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
N448951814001followed by a unit qualifier and the quantityPackage 48951-8140-01. 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)
FOR ORAL USE ONLY
Excerpt only. Read the full label for complete information.
About NDC 48951-8140
- What is NDC 48951-8140?
- 48951-8140 is the product NDC for Rhus Aconitum, Gelsemium sempervirens root 4 [hp_X]/mL + 6 more ingredients liquid, 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?
- Rhus Aconitum.
- What is the active ingredient?
- Gelsemium sempervirens root, Pseudognaphalium luteoalbum leaf, Aconitum napellus, Atropa belladonna, Mandragora officinarum root, Toxicodendron pubescens leaf, Penoxsulam.
- 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 Rhus Aconitum?
- 1 other product NDC are listed under this name. See all Rhus Aconitum NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other Rhus Aconitum products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| Rhus Aconitum | Gelsemium sempervirens root 3 [hp_X]/1 + 6 more ingredients | PelletOral | Uriel Pharmacy Inc. | 48951-8142 | 48951-8142-02 |