What is NDC 43853-0035?

43853-0035 is the product NDC for TestoPRO, Sus scrofa testicle 6 [hp_X]/30mL + 16 more ingredients spray, listed with the FDA by ProBlen. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

TestoPRO (Avena sativa, Damiana, Hamamelis virginiana, Korean ginseng, Populus tremuloides, Baryta carbonica, Hepar suis, Nuphar luteum, Orchitinum suis, Phosphoricum acidum, Sabal serulata, Selenium metallicum, Testosterone, Tribulus terrestris, Horny goat weed, Tongkat ali, Fenugreek).

What is the active ingredient?

Sus scrofa testicle, Phosphoric acid, Saw palmetto, Selenium, Testosterone, Tribulus terrestris whole, Epimedium grandiflorum top, Eurycoma longifolia whole, Fenugreek seed, Avena sativa flowering top, Turnera diffusa leafy twig, Hamamelis virginiana root bark/stem bark, Asian ginseng, Populus tremuloides whole, Barium carbonate, Pork liver, Nuphar lutea root.

ProBlen, NDC labeler code 43853. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for TestoPRO?

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.

TestoPRO NDC 43853-0035 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)43853-0035Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43853-0035Add 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
43853-0035-1	4385300350143853003501	30 mL in 1 BOTTLE (43853-0035-1)Marketed from Jun 28, 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): TestoPRO
Generic name (nonproprietary): avena sativa, damiana, hamamelis virginiana, korean ginseng, populus tremuloides, baryta carbonica, hepar suis, nuphar luteum, orchitinum suis, phosphoricum acidum, sabal serulata, selenium metallicum, testosterone, tribulus terrestris, horny goat weed, tongkat ali, fenugreek
Active ingredients: Sus scrofa testicle — 6 [hp_X]/30mLPhosphoric acid — 12 [hp_X]/30mLSaw palmetto — 6 [hp_X]/30mLSelenium — 12 [hp_X]/30mLTestosterone — 30 [hp_X]/30mLTribulus terrestris whole — 6 [hp_X]/30mLEpimedium grandiflorum top — 6 [hp_X]/30mLEurycoma longifolia whole — 6 [hp_X]/30mLFenugreek seed — 3 [hp_X]/30mLAvena sativa flowering top — 1 [hp_X]/30mLTurnera diffusa leafy twig — 1 [hp_X]/30mLHamamelis virginiana root bark/stem bark — 1 [hp_X]/30mLAsian ginseng — 1 [hp_X]/30mLPopulus tremuloides whole — 1 [hp_X]/30mLBarium carbonate — 8 [hp_X]/30mLPork liver — 6 [hp_X]/30mLNuphar lutea root — 3 [hp_X]/30mL
Dosage form: Spray
Route: Oral
Labeler: ProBlenNDC labeler code 43853
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jun 28, 2017
Listing expires: Dec 31, 2026
DEA schedule: CIII
Other FDA classes: Androgen Receptor Agonists (Mechanism)Androstanes (Chemical structure)
Identifiers: Product ID 43853-0035_eeb44298-3678-344e-e053-2a95a90a8f5fSPL ID eeb44298-3678-344e-e053-2a95a90a8f5fSPL set ID de00895d-db6e-4801-9cfe-a6a4d7235986UNII KM02613O28, E4GA8884NN, J7WWH9M8QS, H6241UJ22B, 3XMK78S47O, 4X4HLN92OT, 137PC46F89, 8GOM182CI3, 654825W09Z, MA9CQJ3F7F, RQ2CFA7WWJ, T7S323PKJS, CUQ3A77YXI, MUN0TBE4PE, 6P669D8HQ8, 6EC706HI7F, 714LIU3V6D
Pharmacologic class: Androgen

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

N443853003501 followed by a unit qualifier and the quantity

Package 43853-0035-01. 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 Nov 30, 2022.

Indications (excerpt from the label)

Uses: Temporarily supports the body to rebalance testosterone output. Symptoms may include: poor muscle/ fat balance, nervousness, feelings of fatigue, poor sleep.*

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 43853-0035

What is NDC 43853-0035?: 43853-0035 is the product NDC for TestoPRO, Sus scrofa testicle 6 [hp_X]/30mL + 16 more ingredients spray, listed with the FDA by ProBlen. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: TestoPRO (Avena sativa, Damiana, Hamamelis virginiana, Korean ginseng, Populus tremuloides, Baryta carbonica, Hepar suis, Nuphar luteum, Orchitinum suis, Phosphoricum acidum, Sabal serulata, Selenium metallicum, Testosterone, Tribulus terrestris, Horny goat weed, Tongkat ali, Fenugreek).
What is the active ingredient?: Sus scrofa testicle, Phosphoric acid, Saw palmetto, Selenium, Testosterone, Tribulus terrestris whole, Epimedium grandiflorum top, Eurycoma longifolia whole, Fenugreek seed, Avena sativa flowering top, Turnera diffusa leafy twig, Hamamelis virginiana root bark/stem bark, Asian ginseng, Populus tremuloides whole, Barium carbonate, Pork liver, Nuphar lutea root.
Who is the labeler?: ProBlen, NDC labeler code 43853. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for TestoPRO?: 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.