Test Flex NDC 49215-0006

NDC codes

FDA NDC Directory

Product NDC (as listed)49215-0006Labeler and product segments. Claims need a package NDC.

Product NDC at billing width49215-0006Add 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
49215-0006-1	49215000601	30 mL in 1 BOTTLE, SPRAY (49215-0006-1)Marketed from Aug 17, 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): Test Flex
Generic name (nonproprietary): avena sativa, calcarea carbonica, damiana, glandula suprarenalis suis, hypophysis suis, magnesia carbonica, millefolium, sabal serrulata, thuja occidentalis, urtica urens
Active ingredients: Avena sativa flowering top — 3 [hp_X]/mLOyster shell calcium carbonate, Crude — 8 [hp_X]/mLTurnera diffusa leafy twig — 3 [hp_X]/mLSus scrofa adrenal gland — 6 [hp_X]/mLSus scrofa pituitary gland — 12 [hp_X]/mLMagnesium carbonate — 8 [hp_X]/mLAchillea millefolium — 6 [hp_X]/mLSaw palmetto — 3 [hp_X]/mLThuja occidentalis leaf — 6 [hp_X]/mLUrtica urens — 3 [hp_X]/mL
Dosage form: Spray
Route: Oral
Labeler: Safe Anabolic Sciences
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Aug 17, 2017
Listing expires: Dec 31, 2026
Identifiers: Product ID 49215-0006_f6a74f50-a725-4b29-8772-a18e76911ca7SPL ID f6a74f50-a725-4b29-8772-a18e76911ca7SPL set ID fed38357-f3b7-42f0-9367-eaf97e15c059UNII MA9CQJ3F7F, 2E32821G6I, RQ2CFA7WWJ, 398IYQ16YV, L0PFEMQ1DT, 0E53J927NA, 2FXJ6SW4PK, J7WWH9M8QS, 0T0DQN8786, IHN2NQ5OF9

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

N449215000601 followed by a unit qualifier and the quantity

Package 49215-0006-01. 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 Aug 17, 2017.

Indications (excerpt from the label)

INDICATIONS: Provides scientifically proven support for temporary relief from many issues experienced by those who want to achieve maximum strength and performance. Benefits may include: • Increased Muscle Mass & Muscle Tone • More Energy • Decreased Bodyfat • Improved Strength • Supports Prostate Health • Enhanced Sex Drive & Performance

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)