Bio Lymph Phase NDC 43742-1667

NDC codes

FDA NDC Directory

Product NDC (as listed)43742-1667Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43742-1667Add 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
43742-1667-1	43742166701	30 mL in 1 BOTTLE, DROPPER (43742-1667-1)Marketed from Aug 7, 2020

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): Bio Lymph Phase
Generic name (nonproprietary): teucrium scorodonia, veronica officinalis, equisetum hyemale, fumaria officinalis, geranium robertianum, nasturtium aquaticum, natrum sulphuricum, pinus sylvestris, gentiana lutea, juglans regia, aranea diadema, sarsaparilla (smilax regelii), ascorbicum acidum, quercetin, scrophularia nodosa, myosotis arvensis, calcarea phosphorica, ferrum iodatum, thyroidinum (suis), gaertner bacillus (bach)
Active ingredients: Teucrium scorodonia flowering top — 3 [hp_X]/mLVeronica officinalis flowering top — 3 [hp_X]/mLEquisetum hyemale whole — 4 [hp_X]/mLFumaria officinalis flowering top — 4 [hp_X]/mLGeranium robertianum whole — 4 [hp_X]/mLNasturtium officinale — 4 [hp_X]/mLSodium sulfate — 4 [hp_X]/mLPinus sylvestris leafy twig — 4 [hp_X]/mLGentiana lutea root — 5 [hp_X]/mLJuglans regia leaf — 5 [hp_X]/mLAraneus diadematus — 6 [hp_X]/mLSmilax ornata root — 6 [hp_X]/mLAscorbic acid — 6 [hp_X]/mLQuercetin — 6 [hp_X]/mLScrophularia nodosa whole — 8 [hp_X]/mLMyosotis arvensis whole — 9 [hp_X]/mLTribasic calcium phosphate — 12 [hp_X]/mLFerrous iodide — 12 [hp_X]/mLThyroid — 12 [hp_X]/mLSalmonella enterica enterica serovar enteritidis — 30 [hp_C]/mL
Dosage form: Liquid
Route: Oral
Labeler: Deseret Biologicals, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Aug 7, 2020
Listing expires: Dec 31, 2026
Other FDA classes: Ascorbic Acid (Chemical structure)Calcium (Chemical structure)Divalent (Chemical structure)Increased Coagulation Factor Activity (Physiologic effect)Phosphate Chelating Activity (Mechanism)
Identifiers: Product ID 43742-1667_53386256-2f45-4db1-8d6f-7288030e8ee5SPL ID 53386256-2f45-4db1-8d6f-7288030e8ee5SPL set ID b7ba12b8-32e2-4e83-a947-d0a1e91e65d1UNII LOK3I16O7G, 9IH82J936J, 59677RXH25, VH659J61ZL, R5I1HK0UBL, YH89GMV676, 0YPR65R21J, Q1RGP4UB73, S72O3284MS, 85HKB87105, 6T6CO7R3Z5, 2H1576D5WG, PQ6CK8PD0R, 9IKM0I5T1E, 7H443NUB2T, C73BK97H5J, 91D9GV0Z28, F5452U54PN, 6RV024OAUQ, Y3V16D4PV4UPC 0810151881683
Pharmacologic class: Blood Coagulation Factor; Phosphate Binder; Vitamin C

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

N443742166701 followed by a unit qualifier and the quantity

Package 43742-1667-01. 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

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