What is NDC 68703-373?

68703-373 is the product NDC for NativeRemedies Backache Ease, Ruta graveolens flowering top 12 [hp_C]/1801 + 8 more ingredients tablet, listed with the FDA by Silver Star Brands. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

NativeRemedies Backache Ease (Arnica, Bryonia, Cimicifuga, Hypericum, Ignatia, Kali carb, Nux vom, Rhus tox, Ruta).

What is the active ingredient?

Ruta graveolens flowering top, Hypericum perforatum, Strychnos nux-vomica seed, Arnica angustifolia flower, Bryonia alba root, Potassium carbonate, Strychnos ignatii seed, Actaea cimicifuga root, Toxicodendron radicans leaf.

Silver Star Brands, NDC labeler code 68703. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for NativeRemedies Backache Ease?

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.

NativeRemedies Backache Ease NDC 68703-373

NDC codes

FDA NDC Directory

Product NDC (as listed)68703-373Labeler and product segments. Claims need a package NDC.

Product NDC at billing width68703-0373Add 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
68703-373-80	6870303738068703037380	180 TABLET in 1 BOTTLE, GLASS (68703-373-80)Marketed from Sep 7, 2021

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): NativeRemedies Backache Ease
Generic name (nonproprietary): arnica, bryonia, cimicifuga, hypericum, ignatia, kali carb, nux vom, rhus tox, ruta
Active ingredients: Ruta graveolens flowering top — 12 [hp_C]/1801Hypericum perforatum — 12 [hp_C]/1801Strychnos nux-vomica seed — 12 [hp_C]/1801Arnica angustifolia flower — 12 [hp_C]/1801Bryonia alba root — 12 [hp_C]/1801Potassium carbonate — 12 [hp_C]/1801Strychnos ignatii seed — 12 [hp_C]/1801Actaea cimicifuga root — 12 [hp_C]/1801Toxicodendron radicans leaf — 12 [hp_C]/1801
Dosage form: Tablet
Route: Oral
Labeler: Silver Star BrandsNDC labeler code 68703
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Sep 7, 2021
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)
Identifiers: Product ID 68703-373_2ab0efa0-68e4-1b30-e063-6294a90ae73eSPL ID 2ab0efa0-68e4-1b30-e063-6294a90ae73eSPL set ID c6259789-438a-211a-e053-2995a90aa5c4UNII N94C2U587S, XK4IUX8MNB, 269XH13919, NG0U89QRD8, T7J046YI2B, BQN1B9B9HA, 1NM3M2487K, 65J267BAZT, CDH3461U7LUPC 0818837015520
Pharmacologic class: 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. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N468703037380 followed by a unit qualifier and the quantity

Package 68703-0373-80. 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 1, 2025.

Indications (excerpt from the label)

Uses*: Uses*: Homeopathic relief of symptoms of backache pain. *Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 68703-373

What is NDC 68703-373?: 68703-373 is the product NDC for NativeRemedies Backache Ease, Ruta graveolens flowering top 12 [hp_C]/1801 + 8 more ingredients tablet, listed with the FDA by Silver Star Brands. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: NativeRemedies Backache Ease (Arnica, Bryonia, Cimicifuga, Hypericum, Ignatia, Kali carb, Nux vom, Rhus tox, Ruta).
What is the active ingredient?: Ruta graveolens flowering top, Hypericum perforatum, Strychnos nux-vomica seed, Arnica angustifolia flower, Bryonia alba root, Potassium carbonate, Strychnos ignatii seed, Actaea cimicifuga root, Toxicodendron radicans leaf.
Who is the labeler?: Silver Star Brands, NDC labeler code 68703. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for NativeRemedies Backache Ease?: 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.