What is NDC 58368-005?

58368-005 is the product NDC for Neorelief For Pain (topical gel for pain), Bellis perennis 4 [hp_X]/g + 21 more ingredients gel, listed with the FDA by BioLyte Laboratories, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Neorelief For Pain (Topical gel for pain).

What is the active ingredient?

Bellis perennis, Bryonia alba root, Calendula officinalis flowering top, Caulophyllum thalictroides root, Causticum, Guaiacum officinale resin, Hypericum perforatum, Lithium carbonate, Frangula californica bark, Rhododendron aureum leaf, Toxicodendron pubescens leaf, Ruta graveolens flowering top, Horse chestnut, Salicylic acid, Black cohosh, Stellaria media, Actaea spicata root, Althaea officinalis root, Arnica montana, Atropa belladonna root, Potassium carbonate, Ledum palustre twig.

BioLyte Laboratories, LLC, NDC labeler code 58368. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Neorelief For Pain?

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.

Neorelief For Pain NDC 58368-005 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)58368-005Labeler and product segments. Claims need a package NDC.

Product NDC at billing width58368-0005Add 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 NDC	11-digit (billing)	Package	Copy
58368-005-01	5836800050158368000501	1 BOTTLE, PUMP in 1 CARTON (58368-005-01) / 56.7 g in 1 BOTTLE, PUMPMarketed from Feb 1, 2017

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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): Neorelief For Pain
Generic name (nonproprietary): topical gel for pain
Active ingredients: Bellis perennis — 4 [hp_X]/gBryonia alba root — 4 [hp_X]/gCalendula officinalis flowering top — 4 [hp_X]/gCaulophyllum thalictroides root — 4 [hp_X]/gCausticum — 4 [hp_X]/gGuaiacum officinale resin — 4 [hp_X]/gHypericum perforatum — 4 [hp_X]/gLithium carbonate — 4 [hp_X]/gFrangula californica bark — 4 [hp_X]/gRhododendron aureum leaf — 4 [hp_X]/gToxicodendron pubescens leaf — 4 [hp_X]/gRuta graveolens flowering top — 4 [hp_X]/gHorse chestnut — 4 [hp_X]/gSalicylic acid — 4 [hp_X]/gBlack cohosh — 4 [hp_X]/gStellaria media — 4 [hp_X]/gActaea spicata root — 4 [hp_X]/gAlthaea officinalis root — 4 [hp_X]/gArnica montana — 4 [hp_X]/gAtropa belladonna root — 4 [hp_X]/gPotassium carbonate — 4 [hp_X]/gLedum palustre twig — 4 [hp_X]/g
Dosage form: Gel
Route: Topical
Labeler: BioLyte Laboratories, LLCNDC labeler code 58368
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Feb 1, 2017
Listing expires: Dec 31, 2027
Identifiers: Product ID 58368-005_4961467c-1d4d-20ce-e063-6394a90a2445SPL ID 4961467c-1d4d-20ce-e063-6394a90a2445SPL set ID 46df076d-4e3a-6faa-e054-00144ff8d46cUNII 2HU33I03UY, T7J046YI2B, 18E7415PXQ, JTJ6HH6YEH, DD5FO1WKFU, N0K2Z502R6, XK4IUX8MNB, 2BMD2GNA4V, 1LZ13MQR0S, IV92NQJ73U, 6IO182RP7A, N94C2U587S, 3C18L6RJAZ, O414PZ4LPZ, K73E24S6X9, 2H03479QVR, 3FU86L9OS0, TRW2FUF47H, O80TY208ZW, 6MW97Q6E8M, BQN1B9B9HA, 877L01IZ0P
Pharmacologic class: Mood Stabilizer

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

N458368000501 followed by a unit qualifier and the quantity

Package 58368-0005-01. 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 Jan 27, 2026.

Indications (excerpt from the label)

Uses For temporary relief of occasional: Minor aches and pains Stiffness of muscles, joints, and tissues Indications are based on homeopathic materia medica, not clinical tests.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 58368-005

What is NDC 58368-005?: 58368-005 is the product NDC for Neorelief For Pain (topical gel for pain), Bellis perennis 4 [hp_X]/g + 21 more ingredients gel, listed with the FDA by BioLyte Laboratories, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Neorelief For Pain (Topical gel for pain).
What is the active ingredient?: Bellis perennis, Bryonia alba root, Calendula officinalis flowering top, Caulophyllum thalictroides root, Causticum, Guaiacum officinale resin, Hypericum perforatum, Lithium carbonate, Frangula californica bark, Rhododendron aureum leaf, Toxicodendron pubescens leaf, Ruta graveolens flowering top, Horse chestnut, Salicylic acid, Black cohosh, Stellaria media, Actaea spicata root, Althaea officinalis root, Arnica montana, Atropa belladonna root, Potassium carbonate, Ledum palustre twig.
Who is the labeler?: BioLyte Laboratories, LLC, NDC labeler code 58368. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Neorelief For Pain?: 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.

Neorelief For Pain (Topical gel for pain) NDC 58368-005