What is NDC 71742-0009?

71742-0009 is the product NDC for Glucose Control T015, Syzygium cumini seed 3 [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?

Glucose Control T015 (Syzygium Jambolanum, Glandula Suprarenalis Suis, Hydrastis Canadensis, Hypophysis Suis, Pancreas Suis, Phaseolus, Aceticum Acidum, Lacticum Acidum, Phosphoricum Acidum, Phosphorus, Uranium Nitricum).

What is the active ingredient?

Syzygium cumini seed, Sus scrofa adrenal gland, Goldenseal, Sus scrofa pituitary gland, Sus scrofa pancreas, Kidney bean, Acetic acid, Lactic acid, Phosphoric acid, Phosphorus, Uranyl nitrate hexahydrate.

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 Glucose Control T015?

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.

Glucose Control T015 NDC 71742-0009

NDC codes

FDA NDC Directory

Product NDC (as listed)71742-0009Labeler and product segments. Claims need a package NDC.

Product NDC at billing width71742-0009Add 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
71742-0009-1	7174200090171742000901	59 mL in 1 BOTTLE, DROPPER (71742-0009-1)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): Glucose Control T015Suffix: T015
Generic name (nonproprietary): syzygium jambolanum, glandula suprarenalis suis, hydrastis canadensis, hypophysis suis, pancreas suis, phaseolus, aceticum acidum, lacticum acidum, phosphoricum acidum, phosphorus, uranium nitricum
Active ingredients: Syzygium cumini seed — 3 [hp_X]/mLSus scrofa adrenal gland — 6 [hp_X]/mLGoldenseal — 6 [hp_X]/mLSus scrofa pituitary gland — 6 [hp_X]/mLSus scrofa pancreas — 6 [hp_X]/mLKidney bean — 9 [hp_X]/mLAcetic acid — 12 [hp_X]/mLLactic acid — 12 [hp_X]/mLPhosphoric acid — 12 [hp_X]/mLPhosphorus — 12 [hp_X]/mLUranyl nitrate hexahydrate — 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: Oct 26, 2017
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Dietary Proteins (Chemical structure)Increased Histamine Release (Physiologic effect)Plant Proteins (Chemical structure)Vegetable Proteins (Chemical structure)
Identifiers: Product ID 71742-0009_5e65d625-8b6c-48af-84c6-f91fdf8cf01dSPL ID 5e65d625-8b6c-48af-84c6-f91fdf8cf01dSPL set ID 3fd02c0a-5cf1-4f35-86d0-d5d09e63f39bUNII 820LSF646I, 398IYQ16YV, ZW3Z11D0JV, L0PFEMQ1DT, 9Y3J3362RY, M98C8416QO, Q40Q9N063P, 33X04XA5AT, E4GA8884NN, 27YLU75U4W, 3V057702FY
Pharmacologic class: 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

N471742000901 followed by a unit qualifier and the quantity

Package 71742-0009-01. 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 Oct 26, 2017.

Indications (excerpt from the label)

INDICATIONS: Pancreas support, blood sugar regulation.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 71742-0009

What is NDC 71742-0009?: 71742-0009 is the product NDC for Glucose Control T015, Syzygium cumini seed 3 [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?: Glucose Control T015 (Syzygium Jambolanum, Glandula Suprarenalis Suis, Hydrastis Canadensis, Hypophysis Suis, Pancreas Suis, Phaseolus, Aceticum Acidum, Lacticum Acidum, Phosphoricum Acidum, Phosphorus, Uranium Nitricum).
What is the active ingredient?: Syzygium cumini seed, Sus scrofa adrenal gland, Goldenseal, Sus scrofa pituitary gland, Sus scrofa pancreas, Kidney bean, Acetic acid, Lactic acid, Phosphoric acid, Phosphorus, Uranyl nitrate hexahydrate.
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 Glucose Control T015?: 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.