Detox NDC 71233-001

NDC codes

FDA NDC Directory

Product NDC (as listed)71233-001Labeler and product segments. Claims need a package NDC.

Product NDC at billing width71233-0001Add 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
71233-001-02	71233000102	59 mL in 1 BOTTLE, DROPPER (71233-001-02)Marketed from Apr 3, 2017

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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
Generic name (nonproprietary): beta vulg, boldo, chelidonium maj, sarsaparilla, gelsemium, veratrum alb, ferrum met, iodium, lycopodium, nux vom, pulsatilla, selenium, thuja occ, zinc met
Active ingredients: Beta vulgaris — 3 [hp_X]/59mLPeumus boldus leaf — 3 [hp_X]/59mLChelidonium majus — 3 [hp_X]/59mLSmilax ornata root — 6 [hp_X]/59mLGelsemium sempervirens root — 7 [hp_X]/59mLVeratrum album root — 7 [hp_X]/59mLIron — 12 [hp_X]/59mLIodine — 12 [hp_X]/59mLLycopodium clavatum spore — 12 [hp_X]/59mLStrychnos nux-vomica seed — 12 [hp_X]/59mLPulsatilla vulgaris — 12 [hp_X]/59mLSelenium — 12 [hp_X]/59mLThuja occidentalis leafy twig — 12 [hp_X]/59mLZinc — 12 [hp_X]/59mL
Dosage form: Liquid
Route: Oral
Labeler: Compass Fat Loss of Glastonbury LLC
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Apr 3, 2017
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)
Identifiers: Product ID 71233-001_d44ac4b5-2283-712b-e053-2a95a90ae6a0SPL ID d44ac4b5-2283-712b-e053-2a95a90ae6a0SPL set ID 927ba08e-54b0-4100-903d-c6f3521ab185UNII 4G174V5051, Q4EWM09M3O, 7E889U5RNN, 2H1576D5WG, 639KR60Q1Q, QNS6W5US1Z, E1UOL152H7, 9679TC07X4, C88X29Y479, 269XH13919, I76KB35JEV, H6241UJ22B, 1NT28V9397, J41CSQ7QDS
Pharmacologic class: Non-Standardized Plant Allergenic Extract

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

N471233000102 followed by a unit qualifier and the quantity

Package 71233-0001-02. 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 Dec 29, 2021.

Indications (excerpt from the label)

Uses Temporarily relieves symptoms related to excretory dysfunction including swollen glands, mucous congestion, digestive problems, gastritis, and allergies.†

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)