Over-the-counter drug · UNAPPROVED HOMEOPATHIC
Respiro-Pro T016 NDC 71742-0010
Ammonium chloride 30 [hp_X]/mL + 8 more ingredients · Liquid · Oral · Guangzhou Renuma Medical Systems Co., Ltd
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 71742-0010-1 | 7174200100171742001001 | 59 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
N471742001001followed by a unit qualifier and the quantityPackage 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.
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.