Detox III NDC 43742-1970

NDC codes

FDA NDC Directory

Product NDC (as listed)43742-1970Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43742-1970Add 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
43742-1970-1	43742197001	30 mL in 1 BOTTLE, DROPPER (43742-1970-1)Marketed from Dec 2, 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): Detox IIISuffix: III
Generic name (nonproprietary): dulcamara, echinacea (angustifolia), aesculus hippocastanum, antimonium tartaricum, ascorbicum acidum, coccus cacti, galium aparine, gentiana lutea, geranium robertianum, pulsatilla (pratensis), sarcolacticum acidum, conium maculatum, lymph node (suis), sulphur, glandula suprarenalis suis, l-phenylalanine, calcarea phosphorica, ferrum phosphoricum, hepar suis, hypothalamus suis, spleen (suis), cortisone aceticum, mercurius solubilis, baryta carbonica, glyphosate, funiculus umbilicalis suis,tonsil (suis),
Active ingredients: Solanum dulcamara top — 4 [hp_X]/mLEchinacea angustifolia whole — 4 [hp_X]/mLHorse chestnut — 6 [hp_X]/mLAntimony potassium tartrate — 6 [hp_X]/mLAscorbic acid — 6 [hp_X]/mLProtortonia cacti — 6 [hp_X]/mLGalium aparine whole — 6 [hp_X]/mLGentiana lutea root — 6 [hp_X]/mLGeranium robertianum whole — 6 [hp_X]/mLPulsatilla pratensis whole — 6 [hp_X]/mLLactic acid, L- — 6 [hp_X]/mLConium maculatum flowering top — 8 [hp_X]/mLSus scrofa lymph — 8 [hp_X]/mLSulfur — 8 [hp_X]/mLSus scrofa adrenal gland — 8 [hp_X]/mLPhenylalanine — 8 [hp_X]/mLTribasic calcium phosphate — 10 [hp_X]/mLFerrosoferric phosphate — 10 [hp_X]/mLPork liver — 10 [hp_X]/mLSus scrofa hypothalamus — 10 [hp_X]/mLSus scrofa spleen — 10 [hp_X]/mLCortisone acetate — 13 [hp_X]/mLMercurius solubilis — 13 [hp_X]/mLBarium carbonate — 28 [hp_X]/mLGlyphosate — 1000 [hp_X]/mLSus scrofa umbilical cord — 6 [hp_C]/mLSus scrofa tonsil — 6 [hp_C]/mLSalmonella enterica subsp. Enterica serovar enteritidis — 9 [hp_C]/mLSus scrofa bone marrow — 12 [hp_C]/mLBisphenol a — 12 [hp_C]/mLBromine — 12 [hp_C]/mLChlorine — 12 [hp_C]/mLHydrofluoric acid — 12 [hp_C]/mLIodine — 12 [hp_C]/mLLiothyronine — 18 [hp_C]/mLEscherichia coli — 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: Dec 2, 2020
Listing expires: Dec 31, 2026
Other FDA classes: Ascorbic Acid (Chemical structure)Calcium (Chemical structure)Divalent (Chemical structure)Corticosteroid Hormone Receptor Agonists (Mechanism)Increased Coagulation Factor Activity (Physiologic effect)Phosphate Chelating Activity (Mechanism)Triiodothyronine (Chemical structure)
Identifiers: Product ID 43742-1970_2ed94953-a1bb-4688-ad02-c956ef2fe32fSPL ID 2ed94953-a1bb-4688-ad02-c956ef2fe32fSPL set ID 6f2136ce-4763-4ebd-a9fc-cbbae1f7ce0bUNII KPS1B1162N, VB06AV5US8, 3C18L6RJAZ, DL6OZ476V3, PQ6CK8PD0R, LZB7TFX1LT, Z4B6561488, S72O3284MS, R5I1HK0UBL, 8E272251DI, F9S9FFU82N, Q28R5GF371, 33A7VYU29L, 70FD1KFU70, 398IYQ16YV, 47E5O17Y3R, 91D9GV0Z28, 91GQH8I5F7, 6EC706HI7F, N6R0856Z79, 92AMN5J79Y, 883WKN7W8X, 324Y4038G2, 6P669D8HQ8, 4632WW1X5A, 118OYG6W3H, TB08NIC03W, Y3V16D4PV4, VP2CN2G7Y8, MLT3645I99, SBV4XY874G, 4R7X1O2820, RGL5YE86CZ, 9679TC07X4, 06LU7C9H1V, 514B9K0L10UPC 0810151880846
Pharmacologic class: Blood Coagulation Factor; Corticosteroid; Phosphate Binder; Vitamin C; l-Triiodothyronine

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

N443742197001 followed by a unit qualifier and the quantity

Package 43742-1970-01. 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 Feb 19, 2024.

Indications (excerpt from the label)

USES: • For the temporary relief of symptoms including: • pain • fatigue • cramping • allergy issues 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)