Flex Drops 2024 (flex drops) NDC 63083-2024

NDC codes

FDA NDC Directory

Product NDC (as listed)63083-2024Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63083-2024Add 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
63083-2024-2	63083202402	59 mL in 1 BOTTLE, DROPPER (63083-2024-2)Marketed from Aug 15, 1985

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): Flex Drops 2024Suffix: 2024
Generic name (nonproprietary): flex drops
Active ingredients: Angelica archangelica root — 2 [hp_X]/59mLAngelica pubescens root — 2 [hp_X]/59mLGambir — 2 [hp_X]/59mLMagnesium phosphate, Dibasic trihydrate — 2 [hp_X]/59mLGuaiac — 3 [hp_X]/59mLPotassium chloride — 3 [hp_X]/59mLManganese — 3 [hp_X]/59mLYucca filamentosa whole — 3 [hp_X]/59mLBryonia alba root — 6 [hp_X]/59mLBovine type ii collagen (Tracheal cartilage) — 6 [hp_X]/59mLCausticum — 6 [hp_X]/59mLRhododendron tomentosum leafy twig — 6 [hp_X]/59mLToxicodendron pubescens leaf — 6 [hp_X]/59mLRuta graveolens flowering top — 6 [hp_X]/59mLLatiglutenase — 8 [hp_X]/59mLOxalic acid — 8 [hp_X]/59mLArnica montana whole — 8 [hp_X]/59mLLatrodectus mactans — 10 [hp_X]/59mL
Dosage form: Liquid
Route: Oral
Labeler: Professional Complementary Health Formulas
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Aug 15, 1984
Listing expires: Dec 31, 2027
Other FDA classes: Increased Large Intestinal Motility (Physiologic effect)Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Inhibition Small Intestine Fluid/Electrolyte Absorption (Physiologic effect)Magnesium Ion Exchange Activity (Mechanism)Osmotic Activity (Mechanism)Osmotic Activity (Mechanism)Potassium Compounds (Chemical structure)Stimulation Large Intestine Fluid/Electrolyte Secretion (Physiologic effect)
Identifiers: Product ID 63083-2024_5d9376a0-da68-43fb-90ad-64fccf77fa33SPL ID 5d9376a0-da68-43fb-90ad-64fccf77fa33SPL set ID e857670f-de84-494e-9e81-80144792d1faUNII DTN01M69SN, 0MF1EI01KJ, 3NJQ5D8S6N, HF539G9L3Q, 03C8A0DFJ8, 660YQ98I10, 42Z2K6ZL8P, T6VR38UJ9I, T7J046YI2B, 76TK29UQEZ, DD5FO1WKFU, 877L01IZ0P, 6IO182RP7A, N94C2U587S, 090PL12YZJ, 9E7R5L6H31, O80TY208ZW, XJJ7QA858R
Pharmacologic class: Calculi Dissolution Agent; Osmotic Laxative; Potassium Salt

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

N463083202402 followed by a unit qualifier and the quantity

Package 63083-2024-02. 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 Jan 8, 2026.

Indications (excerpt from the label)

INDICATIONS For the temporary relief of pain or stiffness in joints, tendons, or muscles.*

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)