NDC codes

FDA NDC Directory
Product NDC (as listed)71742-0010Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71742-0010Add 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
71742-0010-1717420010017174200100159 mL in 1 BOTTLE, DROPPER (71742-0010-1)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)
Respiro-Pro T016Suffix: T016
Generic name (nonproprietary)
ammonium muriaticum, antimonium tartaricum, arsenicum album, bryonia (alba), calcarea carbonica, lobelia inflata, natrum sulphuricum, phosphorus, spongia tosta
Active ingredients
Ammonium chloride — 30 [hp_X]/mLAntimony potassium tartrate — 30 [hp_X]/mLArsenic trioxide — 30 [hp_X]/mLBryonia alba root — 30 [hp_X]/mLOyster shell calcium carbonate, Crude — 30 [hp_X]/mLLobelia inflata — 30 [hp_X]/mLSodium sulfate — 30 [hp_X]/mLPhosphorus — 30 [hp_X]/mLSpongia officinalis skeleton, Roasted — 30 [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 71742-0010_d950f4c8-16f9-4ea0-9535-884e0c2d7816SPL ID d950f4c8-16f9-4ea0-9535-884e0c2d7816SPL set ID 24f5b6f1-a35a-402d-a100-1fb51a5e5a74UNII 01Q9PC255D, DL6OZ476V3, S7V92P67HO, T7J046YI2B, 2E32821G6I, 9PP1T3TC5U, 0YPR65R21J, 27YLU75U4W, 1PIP394IID

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

N471742001001 followed by a unit qualifier and the quantity

Package 71742-0010-01. 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: May temporarily relieve symptoms due to chronic lung disorders, lung inflammation.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 71742-0010

What is NDC 71742-0010?
71742-0010 is the product NDC for Respiro-Pro T016, Ammonium chloride 30 [hp_X]/mL + 8 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?
Respiro-Pro T016 (Ammonium Muriaticum, Antimonium Tartaricum, Arsenicum Album, Bryonia (Alba), Calcarea Carbonica, Lobelia Inflata, Natrum Sulphuricum, Phosphorus, Spongia Tosta).
What is the active ingredient?
Ammonium chloride, Antimony potassium tartrate, Arsenic trioxide, Bryonia alba root, Oyster shell calcium carbonate, Crude, Lobelia inflata, Sodium sulfate, Phosphorus, Spongia officinalis skeleton, Roasted.
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 Respiro-Pro T016?
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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