What is NDC 61727-319?

61727-319 is the product NDC for Hair-X Hair Loss Relief, Cadmium sulfate 12 [hp_C]/4g + 6 more ingredients pellet, listed with the FDA by Homeocare Laboratories. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Hair-X Hair Loss Relief (Cadmium sulfate, Graphite, Phosphoric acid, Silicon dioxide, Selenium, Thallium, Ustilago maydis).

What is the active ingredient?

Cadmium sulfate, Graphite, Phosphoric acid, Silicon dioxide, Selenium, Thallium, Ustilago maydis.

Homeocare Laboratories, NDC labeler code 61727. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Hair-X Hair Loss Relief?

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.

Hair-X Hair Loss Relief NDC 61727-319

NDC codes

FDA NDC Directory

Product NDC (as listed)61727-319Labeler and product segments. Claims need a package NDC.

Product NDC at billing width61727-0319Add 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
61727-319-21	6172703192161727031921	4 g in 1 TUBE (61727-319-21)Marketed from Jul 10, 2012

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): Hair-X Hair Loss Relief
Generic name (nonproprietary): cadmium sulfate, graphite, phosphoric acid, silicon dioxide, selenium, thallium, ustilago maydis
Active ingredients: Cadmium sulfate — 12 [hp_C]/4gGraphite — 4 [hp_C]/4gPhosphoric acid — 5 [hp_C]/4gSilicon dioxide — 4 [hp_C]/4gSelenium — 5 [hp_C]/4gThallium — 7 [hp_C]/4gUstilago maydis — 9 [hp_C]/4g
Dosage form: Pellet
Route: Sublingual
Labeler: Homeocare LaboratoriesNDC labeler code 61727
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jul 10, 2012
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Fungal Proteins (Chemical structure)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)
Identifiers: Product ID 61727-319_7e58d660-4903-5cab-e053-2a91aa0ac70fSPL ID 7e58d660-4903-5cab-e053-2a91aa0ac70fSPL set ID 00b62179-e03b-4972-902d-3a0c969b59bcUNII 947UNF3Z6O, 4QQN74LH4O, E4GA8884NN, ETJ7Z6XBU4, H6241UJ22B, AD84R52XLF, 4K7Z7K7SWGUPC 0361727319210
Pharmacologic class: Non-Standardized Fungal 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. Sublingual products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N461727031921 followed by a unit qualifier and the quantity

Package 61727-0319-21. 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 31, 2018.

Indications (excerpt from the label)

Indications & Usage: Turn tube upside down, twist cap to break seal & release pellets. Using clear cap, place 3 pellets to dissolve under your tongue 3 times a day or as needed. Take apart from food or drinks. To preserve purity avoid touching pellets with fingers.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 61727-319

What is NDC 61727-319?: 61727-319 is the product NDC for Hair-X Hair Loss Relief, Cadmium sulfate 12 [hp_C]/4g + 6 more ingredients pellet, listed with the FDA by Homeocare Laboratories. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Hair-X Hair Loss Relief (Cadmium sulfate, Graphite, Phosphoric acid, Silicon dioxide, Selenium, Thallium, Ustilago maydis).
What is the active ingredient?: Cadmium sulfate, Graphite, Phosphoric acid, Silicon dioxide, Selenium, Thallium, Ustilago maydis.
Who is the labeler?: Homeocare Laboratories, NDC labeler code 61727. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Hair-X Hair Loss Relief?: 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.