Intercellular Detox NDC 62185-0055

NDC codes

FDA NDC Directory

Product NDC (as listed)62185-0055Labeler and product segments. Claims need a package NDC.

Product NDC at billing width62185-0055Add 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
62185-0055-1	62185005501	30 mL in 1 BOTTLE, DROPPER (62185-0055-1)Marketed from Feb 19, 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): Intercellular Detox
Generic name (nonproprietary): ceanothus americanus, argentum nitricum, condurango, hydrastis canadensis, momordica balsamina, pulsatilla (pratensis), bile duct (suis), colon (suis), duodenum (suis), esophagus (suis), eye (suis), gallbladder (suis), ileum (suis), intestine (suis), ipecacuanha, jejunum (suis), kali bichromicum, lung (suis), mucosa nasalis suis, natrum oxalaceticum, oral mucosa (suis), pancreas suis, phosphorus, rectal mucosa (suis), stomach (suis), sulphur, veratrum album, mannose, anacardium orientale, kreosotum,
Active ingredients: Ceanothus americanus leaf — 4 [hp_X]/mLSilver nitrate — 6 [hp_X]/mLMarsdenia condurango bark — 6 [hp_X]/mLGoldenseal — 6 [hp_X]/mLMomordica balsamina immature fruit — 6 [hp_X]/mLPulsatilla pratensis whole — 6 [hp_X]/mLSus scrofa bile duct — 8 [hp_X]/mLSus scrofa colon — 8 [hp_X]/mLSus scrofa duodenum — 8 [hp_X]/mLSus scrofa esophagus — 8 [hp_X]/mLSus scrofa eye — 8 [hp_X]/mLSus scrofa gallbladder — 8 [hp_X]/mLSus scrofa ileum — 8 [hp_X]/mLPork intestine — 8 [hp_X]/mLIpecac — 8 [hp_X]/mLSus scrofa jejunum — 8 [hp_X]/mLPotassium dichromate — 8 [hp_X]/mLSus scrofa lung — 8 [hp_X]/mLSus scrofa nasal mucosa — 8 [hp_X]/mLSodium diethyl oxalacetate — 8 [hp_X]/mLSus scrofa oral mucosa — 8 [hp_X]/mLSus scrofa pancreas — 8 [hp_X]/mLPhosphorus — 8 [hp_X]/mLSus scrofa rectal mucosa — 8 [hp_X]/mLSus scrofa stomach — 8 [hp_X]/mLSulfur — 8 [hp_X]/mLVeratrum album root — 8 [hp_X]/mLMannose, D- — 8 [hp_X]/mLSemecarpus anacardium juice — 9 [hp_X]/mLWood creosote — 10 [hp_X]/mLLachesis muta venom — 10 [hp_X]/mLOxalis acetosella leaf — 10 [hp_X]/mLMandragora officinarum root — 16 [hp_X]/mLSus scrofa urinary bladder — 6 [hp_C]/mLShigella dysenteriae — 30 [hp_C]/mL
Dosage form: Liquid
Route: Oral
Labeler: Dr. Donna Restivo DC
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Feb 19, 2020
Listing expires: Dec 31, 2026
Identifiers: Product ID 62185-0055_79a3f971-033d-4add-a537-9a397d561634SPL ID 79a3f971-033d-4add-a537-9a397d561634SPL set ID 981bc6f9-05da-40cf-9ba0-37acc524f9f8UNII 25B1Y14T8N, 95IT3W8JZE, ZW3Z11D0JV, WUW1665V10, 8E272251DI, 4EE983392U, 94J255A0UC, P6J2SFT80O, 81FZ7X4MWD, X3AOK514E6, B6A98VOI9I, C998R1XSRA, 40GMI0R60L, 62I3C8233L, TA501QD69R, T4423S18FM, 7GL3G1COB3, ID3Z1X61WY, 6CA025Y4FG, DUP6W562BM, 9Y3J3362RY, 27YLU75U4W, 03T60V100Y, T0920P9Z9A, 70FD1KFU70, QNS6W5US1Z, PHA4727WTP, Y0F0BU8RDU, 3JYG22FD73, VSW71SS07I, U1W3U02EW0, I2XCB174VB, 3G7U72W8DA, 1EP6R5562J

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

N462185005501 followed by a unit qualifier and the quantity

Package 62185-0055-01. 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 Jan 18, 2024.

Indications (excerpt from the label)

HOMEOPATHIC INDICATIONS: For the temporary relief of symptoms such as occasional diarrhea, occasional constipation, headaches, gas, congestion, irritated eyes, and indigestion.** **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)