NDC codes

FDA NDC Directory
Product NDC (as listed)70964-0001Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70964-0001Add 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
70964-0001-17096400010130 mL in 1 BOTTLE, SPRAY (70964-0001-1)Marketed from Mar 3, 2017

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)
Advance Plus
Generic name (nonproprietary)
carduus marianus, cynara scolymus, solidago virgaurea, taraxacum officinale, benzoicum acidum, berberis vulgaris, bryonia (alba), cantharis, carduus benedictus, ceanothus americanus, chelidonium majus, chionanthus virginica, cinchona officinalis, dioscorea villosa, dolichos pruriens, iris versicolor, juniperus communis, nux vomica, ptelea trifoliata, uricum acidum
Active ingredients
Milk thistle — 3 [hp_X]/mLCynara scolymus leaf — 3 [hp_X]/mLSolidago virgaurea flowering top — 3 [hp_X]/mLTaraxacum officinale — 3 [hp_X]/mLBenzoic acid — 15 [hp_X]/mLBerberis vulgaris root bark — 15 [hp_X]/mLBryonia alba root — 15 [hp_X]/mLLytta vesicatoria — 15 [hp_X]/mLCentaurea benedicta — 15 [hp_X]/mLCeanothus americanus leaf — 15 [hp_X]/mLChelidonium majus whole — 15 [hp_X]/mLChionanthus virginicus bark — 15 [hp_X]/mLCinchona officinalis bark — 15 [hp_X]/mLDioscorea villosa tuber — 15 [hp_X]/mLMucuna pruriens fruit trichome — 15 [hp_X]/mLIris versicolor root — 15 [hp_X]/mLJuniper berry — 15 [hp_X]/mLStrychnos nux-vomica seed — 15 [hp_X]/mLPtelea trifoliata bark — 15 [hp_X]/mLUric acid — 15 [hp_X]/mL
Dosage form
Spray
Route
Oral
Labeler
VitaminMed, LLCNDC labeler code 70964
Product type
Over-the-counter drug
Marketing category
Unapproved homeopathic
Marketing start
Listing expires
Other FDA classes
Allergens (Chemical structure)Allergens (Chemical structure)Ammonium Ion Binding Activity (Mechanism)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Dietary Proteins (Chemical structure)Food Additives (Chemical structure)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Plant Proteins (Chemical structure)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)
Identifiers
Product ID 70964-0001_71920d36-a413-44e1-9e44-0342d3aea96fSPL ID 71920d36-a413-44e1-9e44-0342d3aea96fSPL set ID 97824fb3-e2b4-4807-943b-88e26b211bf1UNII U946SH95EE, B71UA545DE, 5405K23S50, 39981FM375, 8SKN0B0MIM, 1TH8Q20J0U, T7J046YI2B, 3Q034RO3BT, 6L5ZL09795, 25B1Y14T8N, 7E889U5RNN, S003A158SB, IWY3IWX2G8, 3E271BSI0C, X43D4L3DQC, O84B5194RL, 269XH13919, 5KQR6FTT0D, 268B43MJ25UPC 0744309189461
Pharmacologic class
Nitrogen Binding Agent; 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. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N470964000101 followed by a unit qualifier and the quantity

Package 70964-0001-01. 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)

USES: ■ Improves liver, kidney and colon functions. ■ Reduces symptoms associated with toxic conditions.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 70964-0001

What is NDC 70964-0001?
70964-0001 is the product NDC for Advance Plus, Milk thistle 3 [hp_X]/mL + 19 more ingredients spray, listed with the FDA by VitaminMed, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Advance Plus (Carduus Marianus, Cynara Scolymus, Solidago Virgaurea, Taraxacum Officinale, Benzoicum Acidum, Berberis Vulgaris, Bryonia (Alba), Cantharis, Carduus Benedictus, Ceanothus Americanus, Chelidonium Majus, Chionanthus Virginica, Cinchona Officinalis, Dioscorea Villosa, Dolichos Pruriens, Iris Versicolor, Juniperus Communis, Nux Vomica, Ptelea Trifoliata, Uricum Acidum).
What is the active ingredient?
Milk thistle, Cynara scolymus leaf, Solidago virgaurea flowering top, Taraxacum officinale, Benzoic acid, Berberis vulgaris root bark, Bryonia alba root, Lytta vesicatoria, Centaurea benedicta, Ceanothus americanus leaf, Chelidonium majus whole, Chionanthus virginicus bark, Cinchona officinalis bark, Dioscorea villosa tuber, Mucuna pruriens fruit trichome, Iris versicolor root, Juniper berry, Strychnos nux-vomica seed, Ptelea trifoliata bark, Uric acid.
Who is the labeler?
VitaminMed, LLC, NDC labeler code 70964. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Advance Plus?
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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