Detox NDC 70558-0004

NDC codes

FDA NDC Directory

Product NDC (as listed)70558-0004Labeler and product segments. Claims need a package NDC.

Product NDC at billing width70558-0004Add 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
70558-0004-1	70558000401	30 mL in 1 BOTTLE, DROPPER (70558-0004-1)Marketed from Oct 18, 2018

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
Generic name (nonproprietary): beta vulgaris, boldo, chelidonium majus, sarsaparilla (smilax regelii), gelsemium sempervirens, veratrum album, ferrum metallicum, iodium, lycopodium clavatum, nux vomica, pulsatilla (vulgaris), selenium metallicum, thuja occidentalis, zincum metallicum
Active ingredients: Beta vulgaris whole — 3 [hp_X]/mLPeumus boldus leaf — 3 [hp_X]/mLChelidonium majus whole — 3 [hp_X]/mLSmilax ornata root — 6 [hp_X]/mLGelsemium sempervirens root — 8 [hp_X]/mLVeratrum album root — 8 [hp_X]/mLIron — 12 [hp_X]/mLIodine — 12 [hp_X]/mLLycopodium clavatum spore — 12 [hp_X]/mLStrychnos nux-vomica seed — 12 [hp_X]/mLPulsatilla vulgaris whole — 12 [hp_X]/mLSelenium — 12 [hp_X]/mLThuja occidentalis leafy twig — 12 [hp_X]/mLZinc — 12 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Pro Weight Loss Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Oct 18, 2018
Listing expires: Dec 31, 2027
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 70558-0004_3fb3e7fd-8848-437c-b8d0-d7be176c7ed3SPL ID 3fb3e7fd-8848-437c-b8d0-d7be176c7ed3SPL set ID dbf87fe8-e7c4-4d6f-b55f-da23fcad355eUNII 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

N470558000401 followed by a unit qualifier and the quantity

Package 70558-0004-01. 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 Aug 26, 2026.

Indications (excerpt from the label)

USES: • For the temporary relief of symptoms including: • bladder discomfort • perspiration • expectoration • nasal discomfort • mucus congestion • occasional constipation 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)