NDC codes

FDA NDC Directory
Product NDC (as listed)71742-0012Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71742-0012Add 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
71742-0012-1717420012017174200120159 mL in 1 BOTTLE, DROPPER (71742-0012-1)Marketed from Oct 26, 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)
Spleen-Pro T018Suffix: T018
Generic name (nonproprietary)
spleen (suis), arsenicum album, carbo vegetabilis, ceanothus americanus, chininum sulphuricum, ignatia amara, iodium, natrum muriaticum, nitricum acidum, phosphoricum acidum, phosphorus
Active ingredients
Sus scrofa spleen — 6 [hp_X]/mLArsenic trioxide — 12 [hp_X]/mLActivated charcoal — 12 [hp_X]/mLCeanothus americanus leaf — 12 [hp_X]/mLQuinine sulfate — 12 [hp_X]/mLStrychnos ignatii seed — 12 [hp_X]/mLIodine — 12 [hp_X]/mLSodium chloride — 12 [hp_X]/mLNitric acid — 12 [hp_X]/mLPhosphoric acid — 12 [hp_X]/mLPhosphorus — 12 [hp_X]/mL
Dosage form
Liquid
Route
Oral
Labeler
Guangzhou Renuma Medical Systems Co., LtdNDC labeler code 71742
Product type
Over-the-counter drug
Marketing category
Unapproved homeopathic
Marketing start
Listing expires
Identifiers
Product ID 71742-0012_53f1621b-b6d5-4b35-baf3-1657e67cd5c1SPL ID 53f1621b-b6d5-4b35-baf3-1657e67cd5c1SPL set ID bc2b70bd-2a4a-46fb-b3d8-d69b61056b89UNII 92AMN5J79Y, S7V92P67HO, 2P3VWU3H10, 25B1Y14T8N, KF7Z0E0Q2B, 1NM3M2487K, 9679TC07X4, 451W47IQ8X, 411VRN1TV4, E4GA8884NN, 27YLU75U4W
Pharmacologic class
Antimalarial

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

N471742001201 followed by a unit qualifier and the quantity

Package 71742-0012-01. 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)

INDICATIONS: Spleen support, immune system support.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 71742-0012

What is NDC 71742-0012?
71742-0012 is the product NDC for Spleen-Pro T018, Sus scrofa spleen 6 [hp_X]/mL + 10 more ingredients liquid, listed with the FDA by Guangzhou Renuma Medical Systems Co., Ltd. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Spleen-Pro T018 (Spleen (Suis), Arsenicum Album, Carbo Vegetabilis, Ceanothus Americanus, Chininum Sulphuricum, Ignatia Amara, Iodium, Natrum Muriaticum, Nitricum Acidum, Phosphoricum Acidum, Phosphorus).
What is the active ingredient?
Sus scrofa spleen, Arsenic trioxide, Activated charcoal, Ceanothus americanus leaf, Quinine sulfate, Strychnos ignatii seed, Iodine, Sodium chloride, Nitric acid, Phosphoric acid, Phosphorus.
Who is the labeler?
Guangzhou Renuma Medical Systems Co., Ltd, NDC labeler code 71742. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Spleen-Pro T018?
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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