NDC codes

FDA NDC Directory
Product NDC (as listed)62795-1010Labeler and product segments. Claims need a package NDC.
Product NDC at billing width62795-1010Add 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
62795-1010-26279510100262795101002100 TABLET in 1 BOTTLE (62795-1010-2)Marketed from May 23, 2023
62795-1010-362795101003627951010031 BOTTLE in 1 CARTON (62795-1010-3) / 100 TABLET in 1 BOTTLEMarketed from Jan 1, 2015

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)
BHI Arthritis
Generic name (nonproprietary)
arnica montana root, berberis vulgaris root bark, bryonia alba whole, causticum, citrullus colocynthis fruit pulp, solanum dulcamara top, ferrosoferric phosphate, ledum palustre twig, lycopodium clavatum spore, ranunculus bulbosus, rhododendron aureum leaf, toxicodendron pubescens leaf , and sulfur
Active ingredients
Arnica montana root — 6 [hp_X]/1Berberis vulgaris root bark — 8 [hp_X]/1Bryonia alba whole — 4 [hp_X]/1Causticum — 4 [hp_X]/1Citrullus colocynthis fruit pulp — 5 [hp_X]/1Solanum dulcamara top — 6 [hp_X]/1Ferrosoferric phosphate — 12 [hp_X]/1Ledum palustre twig — 6 [hp_X]/1Lycopodium clavatum spore — 10 [hp_X]/1Ranunculus bulbosus — 8 [hp_X]/1Rhododendron aureum leaf — 6 [hp_X]/1Toxicodendron pubescens leaf — 4 [hp_X]/1Sulfur — 10 [hp_X]/1
Dosage form
Tablet
Route
Oral
Labeler
MediNatura IncNDC labeler code 62795
Product type
Over-the-counter drug
Marketing category
Unapproved homeopathic
Marketing start
Listing expires
Identifiers
Product ID 62795-1010_2e0067b6-5a38-4cbe-845f-c02c9b8f485bSPL ID 2e0067b6-5a38-4cbe-845f-c02c9b8f485bSPL set ID d58c4651-2871-4beb-b1f5-e01a793cbc44UNII MUE8Y11327, 1TH8Q20J0U, 56K0VVT47P, DD5FO1WKFU, 23H32AOH17, KPS1B1162N, 91GQH8I5F7, 877L01IZ0P, C88X29Y479, AEQ8NXJ0MB, IV92NQJ73U, 6IO182RP7A, 70FD1KFU70

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

N462795101002 followed by a unit qualifier and the quantity

Package 62795-1010-02. 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)

USES For the temporary relief of minor arthritis pain, joint stiffness.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 62795-1010

What is NDC 62795-1010?
62795-1010 is the product NDC for BHI Arthritis, Arnica montana root 6 [hp_X]/1 + 12 more ingredients tablet, listed with the FDA by MediNatura Inc. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
BHI Arthritis (ARNICA MONTANA ROOT, BERBERIS VULGARIS ROOT BARK, BRYONIA ALBA WHOLE, CAUSTICUM, CITRULLUS COLOCYNTHIS FRUIT PULP, SOLANUM DULCAMARA TOP, FERROSOFERRIC PHOSPHATE, LEDUM PALUSTRE TWIG, LYCOPODIUM CLAVATUM SPORE, RANUNCULUS BULBOSUS, RHODODENDRON AUREUM LEAF, TOXICODENDRON PUBESCENS LEAF , and SULFUR).
What is the active ingredient?
Arnica montana root, Berberis vulgaris root bark, Bryonia alba whole, Causticum, Citrullus colocynthis fruit pulp, Solanum dulcamara top, Ferrosoferric phosphate, Ledum palustre twig, Lycopodium clavatum spore, Ranunculus bulbosus, Rhododendron aureum leaf, Toxicodendron pubescens leaf, Sulfur.
Who is the labeler?
MediNatura Inc, NDC labeler code 62795. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for BHI Arthritis?
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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