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 NDC11-digit (billing)PackageCopy
43742-1667-1437421667014374216670130 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.NDC labeler code 43742
Product type
Over-the-counter drug
Marketing category
Unapproved homeopathic
Marketing start
Listing expires
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

Current FDA label (SPL), effective .

Indications (excerpt from the label)

USES: • For the temporary relief of symptoms including: • swelling • minor injury These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 43742-1667

What is NDC 43742-1667?
43742-1667 is the product NDC for Bio Lymph Phase, Teucrium scorodonia flowering top 3 [hp_X]/mL + 19 more ingredients liquid, listed with the FDA by Deseret Biologicals, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Bio Lymph Phase (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)).
What is the active ingredient?
Teucrium scorodonia flowering top, Veronica officinalis flowering top, Equisetum hyemale whole, Fumaria officinalis flowering top, Geranium robertianum whole, Nasturtium officinale, Sodium sulfate, Pinus sylvestris leafy twig, Gentiana lutea root, Juglans regia leaf, Araneus diadematus, Smilax ornata root, Ascorbic acid, Quercetin, Scrophularia nodosa whole, Myosotis arvensis whole, Tribasic calcium phosphate, Ferrous iodide, Thyroid, Salmonella enterica enterica serovar enteritidis.
Who is the labeler?
Deseret Biologicals, Inc., NDC labeler code 43742. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Bio Lymph Phase?
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.

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