What is NDC 61727-326?

61727-326 is the product NDC for Eczema Relief, Antimony trisulfide 5 [hp_C]/4g + 8 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?

Eczema Relief (Antimony trisulfide, Apis mellifera, Arsenic trioxide, Atropa belladonna, Graphite, Arctium lappa fruit, Kerosene, Solidago canadensis whole, Viola tricolor).

What is the active ingredient?

Antimony trisulfide, Apis mellifera, Arsenic trioxide, Atropa belladonna, Graphite, Arctium lappa fruit, Kerosene, Solidago canadensis whole, Viola tricolor.

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 Eczema Relief?

2 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Eczema Relief NDC 61727-326 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)61727-326Labeler and product segments. Claims need a package NDC.

Product NDC at billing width61727-0326Add 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
61727-326-21	6172703262161727032621	4 g in 1 TUBE (61727-326-21)Marketed from Jul 6, 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): Eczema Relief
Generic name (nonproprietary): antimony trisulfide, apis mellifera, arsenic trioxide, atropa belladonna, graphite, arctium lappa fruit, kerosene, solidago canadensis whole, viola tricolor
Active ingredients: Antimony trisulfide — 5 [hp_C]/4gApis mellifera — 5 [hp_C]/4gArsenic trioxide — 5 [hp_C]/4gAtropa belladonna — 5 [hp_C]/4gGraphite — 5 [hp_C]/4gArctium lappa fruit — 4 [hp_X]/4gKerosene — 5 [hp_C]/4gSolidago canadensis whole — 4 [hp_X]/4gViola tricolor — 4 [hp_X]/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 6, 2012
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Bee Venoms (Chemical structure)Cell-mediated Immunity (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)
Identifiers: Product ID 61727-326_7e58d849-db30-b924-e053-2991aa0aef01SPL ID 7e58d849-db30-b924-e053-2991aa0aef01SPL set ID 1bfea3be-5909-4aa3-9ec3-05b4db2dd69bUNII F79059A38U, 7S82P3R43Z, S7V92P67HO, WQZ3G9PF0H, 4QQN74LH4O, EA541308MV, 1C89KKC04E, OLL328076K, 9Q24RAI43VUPC 0361727326218
Pharmacologic class: Standardized Insect Venom 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

N461727032621 followed by a unit qualifier and the quantity

Package 61727-0326-21. 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 61727-326

What is NDC 61727-326?: 61727-326 is the product NDC for Eczema Relief, Antimony trisulfide 5 [hp_C]/4g + 8 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?: Eczema Relief (Antimony trisulfide, Apis mellifera, Arsenic trioxide, Atropa belladonna, Graphite, Arctium lappa fruit, Kerosene, Solidago canadensis whole, Viola tricolor).
What is the active ingredient?: Antimony trisulfide, Apis mellifera, Arsenic trioxide, Atropa belladonna, Graphite, Arctium lappa fruit, Kerosene, Solidago canadensis whole, Viola tricolor.
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 Eczema Relief?: 2 other product NDCs are listed under this name. See all Eczema Relief NDCs.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Eczema Relief NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Eczema Reliefcolloidal oatmeal	Oatmeal 10 mg/11g	OintmentTopical	Old East Main Co.	55910-653	55910-0653-34
Eczema Reliefarsenicum iodatum, kali bromatum, kali muriaticum, natrum bromatum, niccolum sulphuricum, sulphur iodatum, viola tricolor, zincum bromatum.	Arsenic triiodide 8 [hp_X]/59mL + 7 more ingredients	LiquidOral	OHM PHARMA INC.	66096-192	66096-0192-05